Pharma company: lupin pharmaceuticals

List of lupin pharmaceuticals products:

• AKT-2
• AKT-FD
• Abel - This medication is used to treat a variety of serious fungal infections. It is often used in patients who cannot tolerate or who do not respond to the regular amphotericin treatment. It works by stopping the growth of fungi.
• Acemiz
• Acemiz-MR
• Akt-3
• Akt-4
• Akurit
• Akurit Kid
• Akurit-3
• Akurit-4
• Akurit-Z
• Akurit-Z Kid
• Alpraquil - Pharmacological action Alpraquil is an anxiolytic drug (tranquilizer), a derivative of triazolo-benzodiazepine. This medication has anxiolytic, sedative, hypnotic, anticonvulsant, central muscle relaxant effect. The mechanism of action is to enhance the inhibitory effect of endogenous GABA in the CNS by increasing the sensitivity of the GABA-receptor mediator as a result of stimulation of benzodiazepine receptors located in the allosteric center of postsynaptic GABA-receptor activating...
• Amigold
• Amikef
• Amlodipine - Amlodipine is a long-acting 1,4-dihydropyridine calcium channel blocker. It acts primarily on vascular smooth muscle cells by stabilizing voltage-gated L-type calcium channels in their inactive conformation. By inhibiting the influx of calcium in smooth muscle cells, amlodipine prevents calcium-dependent myocyte contraction and vasoconstriction. A second proposed mechanism for the drug’s vasodilatory effects involves pH-dependent inhibition of calcium influx via inhibition of smooth...
• Amlodipine; Benazepril - This medication is a combination of two drugs: a calcium channel blocker ( amlodipine ) and an ACE inhibitor ( benazepril ). It is used to treat high blood pressure ( hypertension ). It works by relaxing blood vessels so that blood can flow more easily. Lowering high blood pressure helps prevent strokes, heart attacks and kidney problems.
• Antara Micronized
• Anxicalm - Pharmacological action Alprazolam is an anxiolytic drug (tranquilizer), a derivative of triazolo-benzodiazepine. This medication has anxiolytic, sedative, hypnotic, anticonvulsant, central muscle relaxant effect. The mechanism of action is to enhance the inhibitory effect of endogenous GABA in the CNS by increasing the sensitivity of the GABA-receptor mediator as a result of stimulation of benzodiazepine receptors located in the allosteric center of postsynaptic GABA-receptor activating...
• Arzu
• Atenova - Pharmacological action Atenolol is a cardioselective beta1-blocker without intrinsic sympathomimetic activity. This medication has antihypertensive, antianginal and antiarrhythmic action. Atenolol reduces the stimulatory effect on the heart sympathetic innervation and circulating catecholamines. The hypotensive effect of this drug is associated with a decrease in minute volume of blood, decreased activity of the renin-angiotensin system (has a greater significance for patients with...
• Atenova H
• Atenova-SA
• Azeflo
• Azilup - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Azithromycin inhibits RNA-dependent protein synthesis of sensitive microorganisms. It active against gram-positive bacteria: Staphylococcus aureus, Streptococcus spp. (including Streptococcus pneumoniae, Streptococcus pyogenes group A); gram-negative bacteria: Haemophilus influenzae, Haemophilus parainfluenzae, Haemophilus ducreyi, Moraxella catarrhalis, Escherichia coli, Bordetella pertussis, Bordetella...
• Aziswift - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Azithromycin inhibits RNA-dependent protein synthesis of sensitive microorganisms. It active against gram-positive bacteria: Staphylococcus aureus, Streptococcus spp. (including Streptococcus pneumoniae, Streptococcus pyogenes group A); gram-negative bacteria: Haemophilus influenzae, Haemophilus parainfluenzae, Haemophilus ducreyi, Moraxella catarrhalis, Escherichia coli, Bordetella pertussis, Bordetella...
• Benz
• Budamate Inhaler
• Budamate Transcaps
• Budate
• Budate Respules
• CZ-3
• CZ-Cold
• CZ-L
• Caceff
• Caltop Syrup
• Caltop Tablets
• Caluft
• Canazole - Pharmacological action Clotrimazole is an antifungal agent of imidazole derivatives group for topical use. This medication has an effect at the expense of the synthesis of ergosterol, which is part of the cell membrane of fungi. Clotrimazole has a broad spectrum of action. Clotrimazole is active against dermatophytes, molds, fungi of the genus Candida, Malassezia furfur. This drug is also active against Corynebacterium minutissimum, Streptococcus spp., Staphylococcus spp., Trichomonas...
• Capotril
• Capotril-H
• Carvedilol - Carvedilol information Carvedilol is a blood pressure medication and belongs to the class of drugs known as beta-blockers. These beta-blockers affect the circulatory system, which includes the human heart, arteries and veins. Carvedilol indications This medication is used primarily in treating hypertension or high blood pressure. Carvedilol warnings Taking Carvedilol may not be advisable if you have any of the following conditions: asthma heart problems such as low blood pressure...
• Cefadroxil - SPL UNCLASSIFIED SECTION CEFADROXIL CAPSULES, USP Rev. 01/16 Rx Only To reduce the development of drug resistant bacteria and maintain the effectiveness of cefadroxil capsule and other antibacterial drugs, cefadroxil capsule should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. ...
• Cefantral
• Cefantral-S
• Cefaxone
• Cefdinir - SPL UNCLASSIFIED SECTION To reduce the development of drug-resistant bacteria and maintain the effectiveness of cefdinir and other antibacterial drugs, cefdinir should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION Cefdinir capsules contain the active ingredient cefdinir, an extended-spectrum, semisynthetic cephalosporin,...
• Ceff
• Ceff-ER
• Ceff-LA
• Cefotaxime - SPL UNCLASSIFIED SECTION Rx ONLY PHARMACY BULK PACKAGE – NOT FOR DIRECT INFUSION   To reduce the development of drug-resistant bacteria and maintain the effectiveness of Cefotaxime for Injection, USP...
• Ceftriaxone - SPL UNCLASSIFIED SECTION Rx only To reduce the development of drug-resistant bacteria and maintain the effectiveness of Ceftriaxone for Injection, USP and other antibacterial drugs, Ceftriaxone for Injection, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION ...
• Cefuroxime - PHARMACY BULK PACKAGE NOT FOR DIRECT INFUSION Rx only To reduce the development of drug-resistant bacteria and maintain the effectiveness of Cefuroxime for Injection, USP and other antibacterial drugs, Cefuroxime for Injection, USP should be used only to treat or...
• Celcox - Celecoxib information Celecoxib is a NSAIDs medicine (Non-steroidal anti inflammatory drug). As a NSAID drug, Celecoxib fights against inflammation, pain or swelling by reducing the amount of substances that cause them. Celecoxib indications This medication is usually prescribed to patients who suffer from Stiffness, pain or inflammation which may accompany Osteoarthritis or rheumatoid arthritis. Celecoxib helps ease these symptoms while also decreasing the amount of polyps from your...
• Ceptidar
• Cetil
• Cezolin
• Cilodoc
• Ciprova
• Ciprova-T
• Clamycin
• Clobetavate
• Clopitab
• Clopitab-A
• Coliwell
• Combitaz
• Combunex
• Combutol
• Confal
• Cortina DS
• Cortina SS
• Cyclorin
• Cyclorine
• Dandoff
• Defenac-P
• Defidin
• Defidin-A
• Desloratadine - 1 INDICATIONS AND USAGE Desloratadine Tablets are indicated for: Seasonal Allergic Rhinitis: relief of nasal and non-nasal symptoms in patients 12 years of age and older. ( 1.1 ) Perennial Allergic Rhinitis: relief of nasal and non-nasal symptoms in patients 12 years of age and older. ( 1.2 ) ...
• Dic-OM SR
• Diclonac
• Diclonac SR
• Diclonac-MR
• Diclonac-P
• Diclonova - Pharmacological action NSAIDs, a derivative of phenylacetic acid, diclofenac has a pronounced anti-inflammatory, analgesic and mild antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to two mechanisms: peripheral (indirectly, through suppression of prostaglandin...
• Diclonova MR
• Diclonova P
• Divalproex - This medication is used to treat seizure disorders, certain psychiatric conditions (manic phase of bipolar disorder), and to prevent migraine headaches. It works by restoring the balance of certain natural substances (neurotransmitters) in the brain.
• Dololup - Pharmacological action Piroxicam is a NSAID, refers to a group oxicams. This medication has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action associated with inhibition of the enzyme COX, which leads to inhibition of prostaglandin synthesis from arachidonic acid. Piroxicam inhibits the aggregation of platelets. For systemic use this medicine reduces the pain syndrome. When Piroxicam used externally it weakens or suppresses inflammation and joint pain at rest...
• Doxcef
• Doxcef DT
• Dulot
• Dumore
• E Cef OD
• E-Cef
• Eclor Premix
• Eclor-LA
• Econofix
• Efficin - Magnesium salicylate is used to relieve pain from various conditions. It also reduces pain, swelling, and joint stiffness from arthritis . This medication is known as a nonsteroidal anti-inflammatory drug (NSAID).
• Enthusia
• Ero
• Ero-B
• Eroate - Pharmacological action Erythromycin is a macrolide antibiotic. Has bacteriostatic action. However at higher doses against susceptible organisms has a bactericidal effect. erythromycin is reversibly bound to the ribosome of bacteria, thereby inhibiting protein synthesis. Erythromycin is active against gram-positive bacteria: Staphylococcus spp. (strains producing and not producing penicillinase), Streptococcus spp. (including Streptococcus pneumoniae); gram-negative bacteria: Neisseria...
• Escitalopram - Warnings and Precautions ( 5.2 ) 1/2017 ...
• Esiflo
• Esiflo Inhaler
• Eszopiclone - SPL UNCLASSIFIED SECTION R x only C-IV PRESCRIBING INFORMATION DESCRIPTION: LUNESTA (eszopiclone) is a nonbenzodiazepine hypnotic agent that is a pyrrolopyrazine derivative of the cyclopyrrolone class. The chemical name of eszopiclone is...
• Ethambutol - An antitubercular agent that inhibits the transfer of mycolic acids into the cell wall of the tubercle bacillus. It may also inhibit the synthesis of spermidine in mycobacteria. The action is usually bactericidal, and the drug can penetrate human cell membranes to exert its lethal effect. (From Smith and Reynard, Textbook of Pharmacology, 1992, p863) Indication: For use, as an adjunct, in the treatment of pulmonary tuberculosis. Ethambutol is an oral chemotherapeutic agent which is specifically...
• Ethide
• Eubioz
• Eufox - Pharmacological action Ofloxacin is an antimicrobial agents of broad-spectrum action type from fluoroquinolone group. Bactericidal action of ofloxacin is due to blockage of the enzyme DNA gyrase in bacterial cells. This medication is highly active against most of gram-negative bacteria: Escherichia coli, Salmonella spp., Shigella spp., Proteus spp., Morganella morganii, Klebsiella spp. (including Klebsiella pneumoniae), Enterobacter spp., Serratia spp., Citrobacter spp., Yersinia spp.,...
• Eufox-O
• Eufox-TZ
• Ezedoc
• F-Con - Pharmacological action Fluconazole is an antifungal drug from the group of triazole derivatives. Inhibits the synthesis of ergosterol disrupting the permeability of the cell wall. This medication is active against Candida, Microsporum, Cryptococcus neoformans, Trichophyton. Pharmacokinetics Fluconazole is well absorbed after oral administration. Simultaneous ingestion does not affect absorption. The bioavailability is 90%. Fluconazole is widely distributed in tissues and organs of the...
• FRS
• Famotidine - DESCRIPTION The active ingredient in PEPCID* Registered trademark of Merck Sharp and Dohme Corp, a subsidiary of Merck & Co. Inc. and is used under license. (famotidine) is a histamine H 2 ‑receptor antagonist. Famotidine is N -(aminosulfonyl)-3-[[[2-[(diaminomethylene)amino]-4-thiazolyl]methyl]thio]propanimidamide. The empirical formula of famotidine is C 8 H 15 N 7 O 2 S 3 and its molecular weight is 337.43. Its structural...
• Fastnac
• Faximab
• Ferinova
• Ferinova Capsules
• Ferinova Drops
• Fibril
• Fibril-SF
• Fleta Bolus
• Flucalup - Pharmacological action Fluconazole is an antifungal drug from the group of triazole derivatives. Inhibits the synthesis of ergosterol disrupting the permeability of the cell wall. This medication is active against Candida, Microsporum, Cryptococcus neoformans, Trichophyton. Pharmacokinetics Fluconazole is well absorbed after oral administration. Simultaneous ingestion does not affect absorption. The bioavailability is 90%. Fluconazole is widely distributed in tissues and organs of the...
• Flutiflo
• Fruselac
• Fruselac-DS
• G-Cin
• Gabastar M
• Gatiblu
• Gatiblu-D
• Gatispan
• Gelupin-MPS
• Gemiderm
• Glador
• Gluconorm SR
• Gluconorm-G
• Gluconorm-P
• Glutide-CR
• Helkoss - Pharmacological action Ranitidine is a blocker of histamine H2-receptors. Inhibits basal and stimulated by histamine, gastrin and acetylcholine (to a lesser extent) the secretion of hydrochloric acid. Increases the pH of gastric contents and reduces the activity of pepsin. The duration of action of ranitidine with a single admission - 12 hours. Pharmacokinetics After oral administration, ranitidine is rapidly absorbed from the gastrointestinal tract. Eating and antacids significantly...
• Helkoss-D
• Hepp Forte
• Hepp-Tone
• Imipramine - Imipramine, the prototypical tricyclic antidepressant (TCA), is a dibenzazepine-derivative TCA. TCAs are structurally similar to phenothiazines. They contain a tricyclic ring system with an alkyl amine substituent on the central ring. In non-depressed individuals, imipramine does not affect mood or arousal, but may cause sedation. In depressed individuals, imipramine exerts a positive effect on mood. TCAs are potent inhibitors of serotonin and norepinephrine reuptake. Tertiary amine TCAs, such...
• Ipneb
• Isonorm
• Ixime - Ixime information Ixime is a semi-synthetic cephalosporin antibiotic, destined for oral use, which is able to reduce the development of the drug resistant bacteria. Ixime indications Ixime is usually prescribed by doctors and personal health care providers to patients who are suffering from bacterial infections of the ears, throat, chest, urinary tract and to the individuals who have been diagnosed with the presence of a mild form of gonorrhea. Ixime may also be recommended in the...
• Jolyon-MD
• L-Cin - Levofloxacin information Levofloxacin is type of drug that belongs to the group of medicines called antiepileptic drug. Levofloxacin indications This medication is indicated to control seizure. The precise way of how Levofloxacin works is not yet known. This medicine may also be used for purposes not mentioned here. Levofloxacin warnings This drug belongs in the FDA pregnancy category C. Levofloxacin may cause severe side effects to an unborn baby. Do not take Levofloxacin...
• L-Cin-A
• L-Cin-OZ
• L-Cot
• L-Flox - L-Flox information L-Flox is type of drug that belongs to the group of medicines called antiepileptic drug. L-Flox indications This medication is indicated to control seizure. The precise way of how L-Flox works is not yet known. This medicine may also be used for purposes not mentioned here. L-Flox warnings This drug belongs in the FDA pregnancy category C. L-Flox may cause severe side effects to an unborn baby. Do not take L-Flox medication without consulting first your doctor if...
• LCF
• Lamotrigine - WARNING: SERIOUS SKIN RASHES          See full prescribing information for complete boxed warning. Cases of life-threatening serious rashes, including Stevens-Johnson syndrome and toxic...
• Laxifin
• Lervasc
• Levetiracetam - Levetiracetam information Levetiracetam is type of drug that belongs to the group of medicines called antiepileptic drug. Levetiracetam indications This medication is indicated to control seizure. The precise way of how Levetiracetam works is not yet known. This medicine may also be used for purposes not mentioned here. Levetiracetam warnings This drug belongs in the FDA pregnancy category C. Levetiracetam may cause severe side effects to an unborn baby. Do not take Levetiracetam...
• Levofloxacin - Indications and Usage Plague (1.14) 04/2012 Dosage and Administration Dosage in Adult Patients with Normal Renal Function (2.1) 04/2012 Dosage in Pediatric Patients (2.2) ...
• Lipril - Lisinopril information Lisinopril is a popular drug that belongs to a wide class of medicines generally known as ACE inhibitors (angiotensin converting enzyme inhibitors). This product is generally prescribed to patients who are suffering from congestive heart failure, high blood pressure or to patients who have recently suffered a heart attack. Lisinopril indications This medication is a well known medicine that is generally prescribed to patients who are suffering from heart medical...
• Lipril-AM
• Lipril-H
• Lisinopril; Hydrochlorothiazide - This medication is used to treat high blood pressure ( hypertension ). Lowering high blood pressure helps prevent strokes, heart attacks , and kidney problems. This product contains two medications: lisinopril and hydrochlorothiazide . Lisinopril is an ACE inhibitor and works by relaxing blood vessels so that blood can flow more easily. Hydrochlorothiazide is a "water pill" (diuretic) that causes you to make more urine, which helps your body get rid of extra salt and water. This...
• Losagard
• Losartan - Losartan is an angiotensin-receptor blocker (ARB) that may be used alone or with other agents to treat hypertension. Losartan and its longer acting metabolite, E-3174, lower blood pressure by antagonizing the renin-angiotensin-aldosterone system (RAAS); they compete with angiotensin II for binding to the type-1 angiotensin II receptor (AT1) subtype and prevents the blood pressure increasing effects of angiotensin II. Unlike angiotensin-converting enzyme (ACE) inhibitors, ARBs do not have the...
• Losartan; Hydrochlorothiazide - This drug is used to treat high blood pressure . It is also used to lower the risk of strokes in patients with high blood pressure and an enlarged heart . Lowering high blood pressure helps prevent strokes, heart attacks , and kidney problems. This product contains two medications: losartan and hydrochlorothiazide . Losartan is an angiotensin receptor blocker and works by relaxing blood vessels so that blood can flow more easily. Hydrochlorothiazide is a "water pill" (diuretic) that...
• Lovastatin - DESCRIPTION Lovastatin, USP is a cholesterol lowering agent isolated from a strain of Aspergillus terreus . After oral ingestion, lovastatin, USP, which is an inactive lactone, is hydrolyzed to the corresponding β-hydroxyacid form. This is a principal metabolite and an inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase. This enzyme catalyzes the conversion of HMG-CoA to mevalonate, which is an early and rate limiting step in the...
• Lovex
• Lucipro - Pharmacological action Ciprofloxacin is a broad-spectrum antimicrobial drug of fluoroquinolone group with bactericidal action. Inhibits DNA gyrase and inhibits the synthesis of bacterial DNA. Highly active against most gram-negative bacteria: Pseudomonas aeruginosa, Haemophilus influenzae, Escherichia coli, Shigella spp., Salmonella spp., Neisseria meningitidis, Neisseria gonorrhoeae. Ciprofloxacin is active against Staphylococcus spp. (including strains producing and not producing...
• Lucipro-T
• Lucold
• Lupamik
• Lupenox
• Lupibend
• Lupical
• Lupiderm - Betamethasone information Betamethasone is in a class of drugs called steroids. The medicine reduces swelling and decreases the body's immune response. It is used to treat endocrine (hormonal) disorders when the body does not produce enough of its own steroids. It is also used to treat many immune and allergic disorders, such as arthritis, lupus, psoriasis, asthma, ulcerative colitis, and Crohn's disease. Betamethasone warnings If there is a serious bacterial, viral, or fungal...
• Lupiderm-G
• Lupiderm-GM
• Lupiderm-M
• Lupiderm-S
• Lupidox - Pharmacological action Doxycycline is an semisynthetic tetracycline group's antibiotic of broad-spectrum. This medication has bacteriostatic action due to suppression of protein synthesis of pathogens. It active against aerobic gram-positive bacteria: Staphylococcus spp. (including strains producing penicillinase), Streptococcus spp. (including Streptococcus pneumoniae), Bacillus anthracis, Listeria monocytogenes; anaerobic bacteria: Clostridium spp. Doxycycline is also active against...
• Lupiflam
• Lupiflam-C
• Lupiflex
• Lupigene
• Lupigestrone
• Lupigra
• Lupigyl - Pharmacological action Metronidazole is an anti protozoal agent. It is believed that the mechanism of action is associated with DNA damage-sensitive microorganisms. Active against Trichomonas vaginalis, Gardnerella vaginalis, Giardia lamblia, Entamoeba histolytica, and obligate anaerobic bacteria (including Bacteroides spp., Fusobacterium spp.). Aerobic bacteria are resistant to metronidazole. In combination with amoxicillin Metronidazole is active against Helicobacter pylori. It is...
• Lupihist
• Lupimeb - Pharmacological action Mebendazole is a worming medication a broad spectrum of action, it is most effective when enterobioze. This drug causes irreversible disturbance of glucose utilization in the body of the worm and inhibits the synthesis of ATP. Pharmacokinetics Mebendazole is practically not absorbed from the gastrointestinal tract. The plasma protein binding is 90%. This medication is distributed unevenly in organs and accumulates in adipose tissue, liver, and larvae of helminths...
• Lupimox
• Lupimox Forte
• Lupinace - Enalapril information Enalapril is one of the most effective anti-hypertensive drugs in the market. Belonging to the angiotensin-converting-enzyme inhibitors (ACE inhibitors) category of drugs, Enalapril helps to keep raising blood pressure under control thereby reducing the risk factors of this disease. Since hypertension works out the heart muscles to cause early arterial failure, Enalapril stands in the way and helps to keep your heart healthy, indirectly. Like all other ACE inhibitors,...
• Lupinate
• Lupipan
• Lupipara - Pharmacological action Lupipara is an analgesic-antipyretic. It has analgesic, antipyretic and weak anti-inflammatory action. The mechanism of action is associated with inhibition of prostaglandin synthesis, the predominant influence on the thermoregulation center in the hypothalamus, enhances heat transfer. Why is Lupipara prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in trauma,...
• Lupisetron
• Lupisetron Plus
• Lupispas
• Lupisulide MR
• Lupisulide-D
• Lupisulide-P
• Lupitaz
• Lupiterra
• Lupitros
• Lupivital
• Lupivon
• Lupivon-D
• Lupizole
• Lupome - Pharmacological action Omeprazole is an inhibitor of H+ K+ ATPase. This medication inhibits the activity of H+-K+-ATPase in gastric parietal cells and thus blocks the final stage of hydrochloric acid secretion. This leads to a reduction in basal and stimulated secretion, regardless of the nature of the stimulus. Due to the reduction of acid secretion omeprazole reduces or normalizes the effects of acid in the esophagus in patients with reflux esophagitis. Omeprazole has a bactericidal...
• Lupome-D
• Luprex
• Magnova
• Masdil
• Masdil-OD
• Matilda Forte
• Matilda Plus
• Mefenamic Acid - SPL UNCLASSIFIED SECTION Rx only WARNING: RISK OF SERIOUS CARDIOVASCULAR AND GASTROINTESTINAL EVENTS SPL UNCLASSIFIED SECTION Cardiovascular Thrombotic Events Nonsteroidal anti-inflammatory drugs (NSAIDs) cause an increased...
• Meflup
• Meflup Forte
• Melogesic Mintabs
• Meloxicam - WARNING: RISK OF SERIOUS CARDIOVASCULAR and GASTROINTESTINAL EVENTS Cardiovascular Risk Nonsteroidal anti-inflammatory drugs (NSAIDs) may cause an increased risk of serious cardiovascular (CV) thrombotic events, myocardial infarction, and stroke, which can be fatal. This risk may increase with duration of use....
• Memantine - Memantine is an amantadine derivative with low to moderate-affinity for NMDA receptors. It is a noncompetitive NMDA receptor antagonist that binds preferentially to NMDA receptor-operated cation channels. It blocks the effects of excessive levels of glutamate that may lead to neuronal dysfunction. It is under investigation for the treatment of Alzheimer’s disease, but there has been no clinical support for the prevention or slowing of disease progression. Indication: For the treatment of...
• Merotrol
• Metadrate
• Metformin - Metformin is a biguanide antihyperglycemic agent used for treating non-insulin-dependent diabetes mellitus (NIDDM). It improves glycemic control by decreasing hepatic glucose production, decreasing glucose absorption and increasing insulin-mediated glucose uptake. Metformin is the only oral antihyperglycemic agent that is not associated with weight gain. Metformin may induce weight loss and is the drug of choice for obese NIDDM patients. When used alone, metformin does not cause hypoglycemia;...
• Misobit
• Misolup
• Momeflo
• Moxiblu
• Moxiblu-D
• Moxilup - Pharmacological action Moxilup is an antibiotic of group semisynthetic penicillins a wide spectrum of action. It is a 4-hydroxyl analog of ampicillin. It has bactericidal action. amoxicillin is active against aerobic gram-positive bacteria: Staphylococcus spp. (except strains producing penicillinase), Streptococcus spp; aerobic gram-negative bacteria: Neisseria Gonorrhoeae, Neisseria Meningitidis, Escherichia Coli, Shigella spp., Salmonella spp., Klebsiella spp. Microorganisms producing...
• Mycosure - Pharmacological action Mycosure is an antifungal drug from the group of triazole derivatives. Inhibits the synthesis of ergosterol disrupting the permeability of the cell wall. This medication is active against Candida, Microsporum, Cryptococcus neoformans, Trichophyton. Pharmacokinetics Fluconazole is well absorbed after oral administration. Simultaneous ingestion does not affect absorption. The bioavailability is 90%. Fluconazole is widely distributed in tissues and organs of the...
• Nabumetone - SPL UNCLASSIFIED SECTION Rx Only Cardiovascular Risk NSAIDs Through out this package insert, the term NSAID refers to a non-aspirin non-steroidal anti-inflammatory drug. may cause an increased risk of serious cardiovascular thrombotic events,...
• Nebistar
• Nebistar-SA
• Neucam
• Neucam-P
• Nilup-P
• Nitdin
• Nitdin-TZ
• Nizonide
• Nizonide-O
• Normetic
• Nova Q
• Novakuf
• Novapime
• Novastat
• Odoxil
• Odoxil OD
• Odoxil Premix
• Oloblu
• Omnilup - Pharmacological action Omnilup is an inhibitor of H+ K+ ATPase. This medication inhibits the activity of H+-K+-ATPase in gastric parietal cells and thus blocks the final stage of hydrochloric acid secretion. This leads to a reduction in basal and stimulated secretion, regardless of the nature of the stimulus. Due to the reduction of acid secretion omeprazole reduces or normalizes the effects of acid in the esophagus in patients with reflux esophagitis. Omnilup has a bactericidal effect on...
• One Clav
• Optineuron Injections
• Optineuron Tablets
• Pantolup
• Parovi
• Path - Pharmacological action Pioglitazone is an oral hypoglycemic agent, series of thiazolidinedione derivatives. Powerful and selective agonist of gamma-receptors, peroxisome proliferator-activated (PPAR-gamma). PPAR-gamma receptors are found in adipose and muscle tissues and liver. Activation of nuclear receptor PPAR-gamma modulates the transcription of several genes that are sensitive to insulin, involved in controlling glucose and lipid metabolism. This medicine reduces insulin resistance in...
• Path-G
• Perindopril - Perindopril is a nonsulfhydryl prodrug that belongs to the angiotensin-converting enzyme (ACE) inhibitor class of medications. It is rapidly metabolized in the liver to perindoprilat, its active metabolite, following oral administration. Perindoprilat is a potent, competitive inhibitor of ACE, the enzyme responsible for the conversion of angiotensin I (ATI) to angiotensin II (ATII). ATII regulates blood pressure and is a key component of the renin-angiotensin-aldosterone system (RAAS)....
• Pinom
• Pinom-A
• Pinom-H
• Placidin - Pharmacological action Quetiapine is an antipsychotic (neuroleptic) drug. This medication exhibits a high affinity for serotonin 5HT2-receptors compared with dopamine D1- and D2-receptors in the brain. Also quetiapine has a high affinity for histamine and alpha1-receptors and a less pronounced - to the alpha2-receptors. This drug has no affinity for the m-cholinergic receptors and benzodiazepine receptors. Quetiapine in the dose effectively blocking dopamine D2-receptors causing only weak...
• Placidox
• Pravastatin - Pravastatin is a cholesterol-lowering agent that belongs to a class of medications known as statins. It was derived from microbial transformation of mevastatin, the first statin discovered. It is a ring-opened dihydroxyacid with a 6’-hydroxyl group that does not require in vivo activation. Pravastatin is one of the lower potency statins; however, its increased hydrophilicity is thought to confer advantages such as minimal penetration through lipophilic membranes of peripheral cells,...
• Praxis - Acetylsalicylic acid (ASA) belongs to the group of medications called analgesics (pain relievers), antipyretics (fever reducers), anti-inflammatories ( inflammation reducers), and platelet aggregation inhibitors (anticlotting agents). It works by interfering with the production of compounds in the body that cause pain, fever, inflammation, and blood clots. Acetylsalicylic acid (ASA) is used to relieve pain, fever, and inflammation in various conditions such as lower back and neck...
• Pregabalin - LYRICA is indicated for: LYRICA is indicated for: Neuropathic pain associated with diabetic peripheral neuropathy (DPN) ( 1.1 ) Post herpetic neuralgia (PHN) ( 1.2 ) Adjunctive therapy for adult patients with partial onset...
• Pregastar
• Promet
• Protilup
• Pycof Plus
• Pyralfin
• Pyzin
• Pyzina
• Quinapril - Quinapril is a prodrug that belongs to the angiotensin-converting enzyme (ACE) inhibitor class of medications. It is metabolized to quinaprilat (quinapril diacid) following oral administration. Quinaprilat is a competitive inhibitor of ACE, the enzyme responsible for the conversion of angiotensin I (ATI) to angiotensin II (ATII). ATII regulates blood pressure and is a key component of the renin-angiotensin-aldosterone system (RAAS). Quinapril may be used to treat essential hypertension and...
• Quinlup
• R Clonac
• R-Cin
• R-Cinex
• R-Cinex Z
• R-Cinex-EZ
• RClonac
• RTist
• RTist-DT
• Rablet
• Rablet-D
• Rablet-IT
• Ralofen
• Ramipril - Ramipril information Ramipril belongs to the class of drugs classified as ACE inhibitors or Angiotensin-Converting-Enzyme inhibitor. Ramipril indications This product is a drug prescribed for the treatment of hypertension or high blood pressure, and for the prevention of heart failures succeeding heart attacks. Ramipril is also used for the prevention of heart attacks, stroke and other heart related problems. Ramipril warnings The medication is major allergen especially to patients...
• Ramistar - Ramipril information Ramipril belongs to the class of drugs classified as ACE inhibitors or Angiotensin-Converting-Enzyme inhibitor. Ramipril indications This product is a drug prescribed for the treatment of hypertension or high blood pressure, and for the prevention of heart failures succeeding heart attacks. Ramipril is also used for the prevention of heart attacks, stroke and other heart related problems. Ramipril warnings The medication is major allergen especially to patients...
• Ramistar-A
• Ramistar-H
• Rcifax
• Rcinex-E
• Rcinex-Z
• Reclav
• Recovit
• Resner
• Retorlix
• Ribafit
• Ribavin
• Ributin
• Rifabutin - DESCRIPTION MYCOBUTIN Capsules for oral administration contain 150 mg of the rifamycin antimycobacterial agent rifabutin, USP, per capsule, along with the inactive ingredients microcrystalline cellulose, magnesium stearate, red iron oxide, silica gel, sodium lauryl sulfate, titanium dioxide, and edible white ink. The chemical name for rifabutin is 1',4-didehydro-1-deoxy-1,4-dihydro-5'-(2-methylpropyl)-1-oxorifamycin XIV (Chemical Abstracts...
• Rifagut
• Rifzin F
• Rinizide
• Rinizide Forte DT
• Romento - Pharmacological action Romento is a medication for the treatment of erectile dysfunction. This drug restores impaired erectile function and provides a natural response to sexual stimulation. Sildenafil is a potent and selective inhibitor of cGMP-specific phosphodiesterase type 5 (PDE5) which is responsible for the breakdown of cGMP in the cavernous body. This medicine has no direct relaxing effect on corpus cavernosum, but enhances the relaxing effect of active nitric oxide in this tissue....
• Rumibex
• Salbair - Pharmacological action Albuterol Pharmaceuticals is a beta adrenoagonists with a predominant effect on beta2-adrenergic receptors (localized, particularly in the bronchi, myometrium, blood vessels). This medication prevents and reduces or eliminates bronchospasm, reduces the resistance in the airways, increases the vital capacity. It prevents the release of histamine, slow reacting substance from mast cells and factors chemotaxis of neutrophils. Compared with other drugs of this group has...
• Salbair B Forte
• Salbair Respules - Pharmacological action Albuterol Pharmaceuticals is a beta adrenoagonists with a predominant effect on beta2-adrenergic receptors (localized, particularly in the bronchi, myometrium, blood vessels). This medication prevents and reduces or eliminates bronchospasm, reduces the resistance in the airways, increases the vital capacity. It prevents the release of histamine, slow reacting substance from mast cells and factors chemotaxis of neutrophils. Compared with other drugs of this group has...
• Salbair-B
• Salbair-I
• Signoflam
• Simvastatin - Pharmacological action Simvastatin is a hypolipidemic agent from a group of statins, an inhibitor of HMG-CoA reductase. This medication is a prodrug because it has in its structure the closed lactone ring which is hydrolyzed after intake. Lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. Reducing cholesterol is dose-dependent and is not linear but exponential. Statins do not affect the activity of lipoprotein and hepatic lipase, have no...
• Softovac
• Softovac-SF
• Solubet - Betamethasone information Betamethasone is in a class of drugs called steroids. The medicine reduces swelling and decreases the body's immune response. It is used to treat endocrine (hormonal) disorders when the body does not produce enough of its own steroids. It is also used to treat many immune and allergic disorders, such as arthritis, lupus, psoriasis, asthma, ulcerative colitis, and Crohn's disease. Betamethasone warnings If there is a serious bacterial, viral, or fungal...
• Sparflin
• Stalopam
• Stalopam Plus
• Starcad
• Starcet
• Starcet Cold
• Starcet-A
• Starstat - Pharmacological action Atorvastatin is a lipid-lowering drugs of the statin group. An inhibition of HMG-CoA reductase leads to a series of sequential reactions that result in reduced intracellular cholesterol content and it is a compensatory increase in activity of LDL receptors and thus accelerate the catabolism of LDL cholesterol. The lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. The reduction in LDL cholesterol is dose-dependent and is...
• Starstat-EZ
• Stressban Alprazolam - Pharmacological action Stressban Alprazolam is an anxiolytic drug (tranquilizer), a derivative of triazolo-benzodiazepine. This medication has anxiolytic, sedative, hypnotic, anticonvulsant, central muscle relaxant effect. The mechanism of action is to enhance the inhibitory effect of endogenous GABA in the CNS by increasing the sensitivity of the GABA-receptor mediator as a result of stimulation of benzodiazepine receptors located in the allosteric center of postsynaptic GABA-receptor...
• Stressban Nitrazepam
• Suprax - Cefixime is an antibiotic that belongs to the family of medications known as cephalosporins . It is used to treat certain types of bacterial infections. It is most commonly used to treat gonorrhea as well as infections of the ear, sinus, bladder, throat, and lung. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used for all of the conditions discussed here. If you...
• Supraxone
• Supraxone-S
• Tazar
• Tazox
• Tegaspa
• Teguphen
• Telekast
• Telekast-L
• Telista
• Telista-H
• Telista-RM
• Tiate
• Timoblu
• Tiomate
• Tirofuse
• Tonact - Pharmacological action Atorvastatin is a lipid-lowering drugs of the statin group. An inhibition of HMG-CoA reductase leads to a series of sequential reactions that result in reduced intracellular cholesterol content and it is a compensatory increase in activity of LDL receptors and thus accelerate the catabolism of LDL cholesterol. The lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. The reduction in LDL cholesterol is dose-dependent and is...
• Tonact Forte
• Tonact Plus
• Tonact-ASP
• Tonact-EZ
• Tonact-TG
• Topiramate - DESCRIPTION Topiramate is a sulfamate-substituted monosaccharide. Topiramate tablets are available as 25 mg, 50 mg, 100 mg, and 200 mg circular tablets for oral administration. Topiramate is a white crystalline powder with a bitter taste. Topiramate USP is most soluble in alkaline solutions containing sodium hydroxide or sodium phosphate and having a pH of 9 to 10. It is freely soluble in acetone, chloroform, dimethylsulfoxide, and ethanol....
• Topol-XL - Pharmacological action Metoprolol is a cardioselective beta1-blocker without intrinsic sympathomimetic activity. This medication has antihypertensive, antianginal and antiarrhythmic effect. Metoprolol decreases automaticity of sinus node, reducing heart rate, slows AV-conduction, decreases myocardial contractility and excitability, reduces cardiac output, reduces myocardial oxygen demand. This drug inhibits the stimulatory effect of catecholamines on the heart during physical and...
• Torolac
• Trandolapril - WARNING: FETAL TOXICITY When pregnancy is detected, discontinue trandolapril as soon as possible. Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus. (See WARNINGS : Fetal Toxicity .) DESCRIPTION Trandolapril is the ethyl ester prodrug of a nonsulfhydryl...
• Tusant
• Utibid
• Val-BCD
• Valbet Cream
• Valbet Scalp Application
• Valent
• Valent R
• Valent-H
• Vida
• Vida-H
• Viramid - Lamivudine information Lamivudine is an anti-HIV treatment in the class of drugs called Nucleoside Reverse Transcriptase Inhibitors (NRTIs). The body breaks down these drugs into chemicals that stop HIV from infecting uninfected cells in the body, but they do not help cells that have already been infected with the virus. This product is an important part of combination anti-HIV treatment. Lamivudine inhibits the reproduction of viruses in the body. Lamivudine warnings Before taking the...
• Virazide
• Vitalup
• Vobit
• Voritrol
• Wowrab
• X-Ceff
• X-LCF
• Ximeceff - Ximeceff information Ximeceff is a semi-synthetic cephalosporin antibiotic, destined for oral use, which is able to reduce the development of the drug resistant bacteria. Ximeceff indications Ximeceff is usually prescribed by doctors and personal health care providers to patients who are suffering from bacterial infections of the ears, throat, chest, urinary tract and to the individuals who have been diagnosed with the presence of a mild form of gonorrhea. Ximeceff may also be...
• Xoneceff

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The information was verified by Dr. Rachana Salvi, MD Pharmacology