46 Products

in Tablets

5-ZINE-A Tablets

- LEVOCETIRIZINE 2.5mg

- AMBROXOL 60mg

- PHENYLEPHRINE 5mg

- PCM 325mg

5-ZINE-D Tablets

- PARACETAMOL 325mg

- PHENYLEPHRINE 5 mg HCI

- CAFFEINEEE 30mg

- DIPHENHYDRAMINE 25mg

5 Zine Tablet

- LEVOCETIRIZINE 5mgUses Levocetirizine is an antihistamine used to relieve allergy symptoms such as watery eyes

- runny nose

- itching eyes/nose

- sneezing

5-ZINE-P Tablets

- PCM 325mg

- CHLORPHENIRAMINE MALEATE 2mg

- PHENYLEPHRINE HCL5mg

- CAFFEINE16mg

ACRIN-G Tablets

- DIACERIN 50mg

- GLUCOSAMINE 750mg

- MSM 200mg

- MULTIVITAMIN

BAREC-20 Tablets

- BAREC (RABEPRAZOLE 20 MG) is used to treat certain stomach and esophagus problems (such as acid reflux

- ulcers). It works by decreasing the amount of acid your stomach makes. It relieves symptoms such as heartburn

- difficulty swallowing

- and persistent cough PHARMACOLOGY PHARMACODYNAMICS: Mechanism of Action: – Rabeprazole sodium belongs to the class of anti-secretory compounds

CHETRE-BRD Tablets

- TRYPSIN 48mg

- BROMELAIN 90mg

- RUSTOSIDE 100mg

- DICLOFENAC 50mgPHARMACOLOGYA.) PHARMACODYNAMICS: On being absorbed

CONZIP-150 Tablets

- Fluconazole is used to treat vaginal yeast infections. It works by stopping the growth of common types of vaginal yeast (fungus). This medication belongs to a class of drugs called azole antifungals. How to use Fluconazole Tablet Azole Antifungals-Systemic Read the Patient Information Leaflet before you start taking fluconazole and each time you get a refill. If you have any questions

- ask your doctor or pharmacist. In Canada

- some brands of this medication are available without a prescription. Before taking over-the-counter fluconazole

- read the product instructions and talk to your doctor if this is your first vaginal yeast infection

CORAFLAV Tablets

- A drug that has been used in various urinary syndromes and as an antispasmodic. It may have local anesthetic activity and direct relaxing effects on smooth muscle as well as some activity as a muscarinic antagonist. Pharmacodynamics: - Flavoxate is a spasmolytic flavone derivative that acts by relaxing the smooth muscle in the urinary tract. Flavoxate is a competitive muscarinic receptor antagonist indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence

- urgency

- and urinary frequency. Muscarinic receptors play an important role in several major cholin-ergically mediated functions

- including contractions of urinary bladder smooth muscle and stimulation of salivary secretion. Mechanism of action Flavoxate acts as a direct antagonist at muscarinic acetylcholine receptors in cholinergically innervated organs. Its anticholinergic-parasympatholytic action reduces the tonus of smooth muscle in the bladder

Csog Tablets

- CALCIUM CITRATE 1000mg

- MAGNESIUM HYDROCHLORIDE 100mg

- ZINC 4mg

- VITAMIND3 200 I.UThis combination medication is used to prevent or treat low blood calcium levels in people who do not get enough calcium from their diets. It may be used to treat conditions caused by low calcium levels such as bone loss (osteoporosis)

DOCRU-TH Tablets

- ETORICOXIB 60mg

- THIOCOLCHICOSIDE 4mg

EMDAR Tablets

- ONDENSETRON 4mg

- MOUTH DISSOLVING TABLETS

FAXLI-500 Tablets

- LEVOFLOXACIN 500mgPHARMACODYNAMICS: - Levofloxacin

- a fluoroquinolone antiinfective

- is the optically active L-isomer of ofloxacin. Levofloxacin is used to treat bacterial conjunctivitis

- sinusitis

FEXMARE Tablets

- FEXOFENADINE120mg

- MONTELUKAST10mgMetabolism May Be Increased With Rifampicin

- Phenobarbital

- Phenytoin. Peripheral Oedema May Occur With Prednisone. Mechanism of Action of Montelukast 10mg + Fexofenadine 120mg: Montelukast Is A Selective Leukotriene Receptor Antagonist That Blocks The Effects Of Cysteinyl Leukotrienes In The Airways. Absorption: Rapidly Absorbed From The GI Tract (Oral).Peak Plasma Concentrations In 2-4 Hr. Mean Oral Bioavailability: 64%. Distribution: Protein-Binding: >99%. Metabolism: Extensively Hepatic By CYP3A4

FYCEF-100 Tablets

- Cefixime

- an antibiotic

- is a third-generation cephalosporin like ceftriaxone and cefotaxime. Cefixime is highly stable in the presence of beta-lactamase enzymes. As a result

- many organisms resistant to penicillins and some cephalosporins due to the presence of beta-lactamases

FYCEF-200 Tablets

- Cefixime

- an antibiotic

- is a third-generation cephalosporin like ceftriaxone and cefotaxime. Cefixime is highly stable in the presence of beta-lactamase enzymes. As a result

- many organisms resistant to penicillins and some cephalosporins due to the presence of beta-lactamases

FYCEF-AZ LB Tablets

- BRAND NAME: - FYCEF-AZ LBCOMPOSITION: - CEFIXIME 200 mg + AZITHROMYCIN 250 mg + LACTIC ACID BACILLUS 60 MILLION SPORESPACKING: - 10X1X10 (ALU-ALU)M.R.P: - 2200/-A new combination of CEFIXIME AND AZITHROMYCIN is used for the treatment of upper and lower respiratory tract infection. Cefixime

- an antibiotic

- is a third-generation cephalosporin like ceftriaxone and cefotaxime. Cefixime is highly stable in the presence of beta-lactamase enzymes. As a result

- many organisms resistant to penicillins and some cephalosporins due to the presence of beta-lactamases

FYCEF-CV Tablets

- CEFIXIME 200mg

- CLAVUNIC ACID 125mgCefixime

- an antibiotic

- is a third-generation cephalosporin like ceftriaxone and cefotaxime. Cefixime is highly stable in the presence of beta-lactamase enzymes. As a result

FYCEF-LB Tablets

- CEFIXIME 200mg

- LACTIC ACID BACILLUS 2.5BILLIONCefixime

- an antibiotic

- is a third-generation cephalosporin like ceftriaxone and cefotaxime. Cefixime is highly stable in the presence of beta-lactamase enzymes. As a result

FYCEF-O LB Tablets

- BRAND NAME: - FYCEF-O LBCOMPOSITION: - CEFIXIME 200 mg + OFLOXACIN 200 mg + LACTIC ACID BACILLUS 60 MILLION SPORESPACKING: - 10X1X10 (ALU-ALU)M.R.P: - 1790/-CEFIXIME 200 mg:  - Cefixime is an antibiotic. It kills the bacteria by attacking their cell wall. Specifically

- it prevents the synthesis of a substance in the cell wall called peptidoglycan

- which provides the cell wall with the strength required for survival of bacteria in human body.Cefixime is an orally active third generation bactericidal cephalosporin with broad spectrum of coverage. Cefixime has been shown to be active against most strains of the Gram-positive organisms. As with other cephalosporins

- bactericidal action of cefixime results from inhibition of bacterial cell- wall synthesis. The peptidoglycan layer is important for cell wall structural integrity.OFLOXACIN 200 mg: - Ofloxacin is associated with an increased risk of tendon problems. These include pain

FYCEF-O Tablets

- CEFIXIME 200mg

- OFLOXACIN 200mgCefixime is an orally active 3rd generation cephalosporin which exerts its bactericidal action against both gram positive & gram negative organisms by inhibiting bacterial cell wall synthesis. Cefixime inhibits transpeptidase & thus prevents cross linking of bacterial cell wall. Transpeptidase & associated proteins constitute various types of specific binding proteins which have affinity for cephalosporins like Cefixime. It is highly active against enterobacteriaceae

- Haemophilus influenzae

- Streptococcus pyogens & Streptococcus pneumonia &many beta lactamase producing bacteria. Ofloxacin is a bactericidal drug. It act by inhibiting the enzyme DNA gyrase (Topoisomerase 2) and Topoisomerase 4.DNA gyrase helps in the formation of a highly condensed three dimensional structure of the DNA by its nicking and closing activity and also by introducing negative supercoil in to the DNA double helix. Ofloxacin inhibits DNA gyrase which results in abnormal linkage between opened DNA and gyrase and negative supercoiling is also impaired. This will inhibits transcription of DNA in to RNA and subsequent protein synthesis. Lactic Acid Bacillus - Protects & restores the intestinal microflora - Prevents diarrhoea & dyspepsia - Maintains the intestinal pH & inhibits the growth of pathogens

LINEWAR 600 Tablets

- COMPOSITION: -LINEZOLID 600 MG Packing: - 10X1X4 M.R.P: - 2400PHARMACOLOGY PHARMACOKINETICS: Absorption: Owing to hepatic first-pass metabolism

- its bioavailability is only about 60%. Distribution: Plasma protein binding of ondansetron as measured in vitro was 70% to 76%

- over the pharmacologic concentration range of 10 to 500 ng/mL. Circulating drug also distributes into erythrocytes. Metabolism: Ondansetron is extensively metabolized in humans

- with approximately 5% of a radiolabeled dose recovered as the parent compound from the urine. The primary metabolic pathway is hydroxylation on the indole ring followed by subsequent glucuronide or sulfate conjugation. Elimination: In adult cancer patients

MEBEZON Tablets

- MEBEVERINE HCL 135mg & CHLORDIAZEPOXIDE 5mg Packing: -10X10 M.R.P: - 1100Mebeverine HCl is a musculotropic antispasmodic drug without atropic side-effects whose major therapeutic role is in the treatment of irritable bowel syndrome. It is also indicated for treatment of gastrointestinal spasm secondary to organic disorder. Chlordiazepoxide is a sedative/hypnotic drug and benzodiazepine derivative. Chlordiazepoxide has a medium to long half life but its active metabolite has a very long half life. The drug has amnestic

- anxiolytic

- hypnotic and skeletal muscle relaxant properties. PHARMACOKINETICS MEBEVERINE ABSORPTION: – Rapidly absorbed from the GI tract (oral); peak plasma concentrations within 1-3 hr.DISTRIBUTION: – Protein-binding: 75% to albumin. METABOLISM: – Hydrolysed completely in the liver to veratric acid and mebeverine alcohol. EXCRETION: – Via urine (as metabolites). CHLORDIAZEPOXIDE ABSORPTION: – Rapidly absorbed following oral administration. PROTEIN BINDING: – Approximately 40% bound to plasma proteins. METABOLISM: – Chlorothiazide is not metabolized but is eliminated rapidly by the kidney.EXCRETION: – Chlorothiazide is not metabolized but is eliminated rapidly by the kidney. After oral doses

- 10 to 15 percent of the dose is excreted unchanged in the urine. Chlorothiazide crosses the placental but not the blood-brain barrier and is excreted in breast milk. HALF-LIFE: – 45-120 minutesPHARMACODYNAMICS:- Mebeverine is a musulotrophic antispasmodic with a direct effect on the smooth muscle of the gastro-intestinal tract

MYZEP-D Tablets

- DICLOFENAC POTASSIUM 50mg

- SERRATIOPEPTIDASE 10mg

NERVER-GB Tablets

- MECOBALAMIN 500 MG & GABAPENTIN 300 MG Packing: - 10x10 M.R.P: -1050Methylcobalamin and Gabapentin combination is useful for the treatment of neuropathic disorders or seizure disorders. Gabapentin can also be used to treat partial seizures in children between the ages of three and 12. Methylcobalamin is a form of vitamin B that is used to prevent postherpetic neuralgia

- neuralgia intercostals

- and diabetic neuropathy. Gabapentin is an anti-convulsant that prevents repeated electrical signals in the brain that cause seizures and is used to treat epilepsy or other similar disorders.

NERVER Tablets

- MECOBALAMIN 1500mcg

- ALA 300mg

- VITAMIN B2 10mg

- B6 3mg

NIZBRO-200 SR Tablets

- ACEBROPHYLLINE 200 MG Packing: -10X10 M.R.P: - 1420ACEBROPHYLLINE HAS 3 ACTIONS NAMELY BRONCHODILATION

- MUCOREGULATION & ANTI-INFLAMMATORY ACTION. PHARMACOLOGY A.) PHARMACODYNAMICS: Acebrophylline inhibits intracellular phosphodiesterase associated significantly reduce the airway inflammation and obstruction in chronic stages. Acebrophylline increases the synthesis and release of alveolar surfactant

- resulting in triple action: mucoregulation

- stimulation of bronchoalveolar clearance

PENSIG Tablets

- PANTOPRAZOLE 40 MG Packing: - 10X10 M.R.P: -550PANTOPRAZOLE 40 MG is a proton pump inhibitor drug used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease. It can be used as a maintenance therapy for long term use after initial response is obtained. Pharmacokinetics Pantoprazole inhibits H+/K+ ATPase pump function thereby reducing gastric acid secretion. It also has a role in the eradication of H. pylori. Absorption : -Well absorbed; peak plasma concentrations: Approx 2-2.5 hr after oral dose. Oral bioavailability: Approx 77% with enteric-coated formulation (does not vary after single or multiple doses). Distribution Protein-binding: 98%; volume of distribution: 11-24 L. Metabolism Hepatic; mainly by cytochrome CYP2C19 and slightly by CYP2D6 and CYP2C0. Excretion Via urine (approx 80%) and bile (approx 20%).Elimination half life: approx 1 hour (prolonged in hepatic impairment; in patients with cirrhosis the elimination half life may be 3-10 hours).

PENSIG-D Tablets

- PANTOPRAZOLE 40 MG & DOMPERIDONE 10 MG Packing: -10X10 M.R.P: - 650PANTOPRAZOLE 40 MG & DOMPERIDONE 10 MG: - Pantoprazole is a proton pump inhibitor drug used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease whereas Domperidone is a specific blocker of dopamine receptors. It speeds gastrointestinal peristalsis

- causes prolactin release

- and is used as antiemetic.Pantoprazole acts by selectively inhibiting the H+/K+-ATPase enzyme in the secretory canaliculus of the stimulated parietal cell. Domperidone stimulates GI activity by acting as a competitive antagonist at dopamine D2-receptors. Pharmacology: Pantoprazole: Pantoprazole is a proton pump inhibitor (PPI) that suppresses the final step in gastric acid production. Pantoprazole is unstable in acid and is administered orally in the form of an enteric-coated tablet Pantoprazole is completely and rapidly absorbed after oral administration. The absolute bioavailability from the tablet was found to be about 77 %. Pantoprazole is extensively metabolized in the liver through the cytochrome P450 (CYP) system.Renal elimination represents the major route of excretion (about 80%) for the metabolites of Pantoprazole; the rest is excreted with the faeces. Domperidone: Domperidone acts as a gastrointestinal emptying (delayed) adjunct and peristaltic stimulant. The gastroprokinetic properties of Domperidone are related to its peripheral dopamine receptor blocking properties.. In fasting subjects

- Domperidone is rapidly absorbed after oral administration. Domperidone is 91-93% bound to plasma proteins. Domperidone undergoes rapid and extensive hepatic metabolism and Urinary and faecal excretions amount to 31 and 66% of the oral dose respectively. Indications:Antacids Antireflux Agents & Antiulcerants / GIT Regulators

PODZY-200 Tablets

- CEFPODOXIME 200 MG Packing: - 10X10 M.R.P: -2490Cefpodoxime is an oral third generation cephalosporin antibiotic. It is active against most Gram positive and Gram negative bacteria. It is commonly used to treat acute otitis media

- pharyngitis

- and sinusitis. Cefpodoxime proxetil is a prodrug which is absorbed and de-esterified by the intestinal mucosa to Cefpodoxime. PHARMACODYNAMICS: - Cefpodoxime is an oral third generation cephalosporin antibiotic. It is active against most Gram positive and Gram negative bacteria. Notable exceptions include Pseudomonas aeruginosa

- Enterococcus

PODZY-CV Tablets

- CEFPODOXIME 200 MG + CLAVUNANIC ACID 125 MGPacking: - 1X10 M.R.P: -270Cefpodoxime and Clavulanic acid combination are effective against multiple infections. The pharmacological action of Clavulanic acid prevents hydrolysis of Cefpodoxime against beta-lactamase secreting microbes and increases the antibiotic spectrum. Cefpodoxime

- an antibiotic belongs to class of third-generation cephalosporins

- is indicated for the treatment of systemic infections including respiratory tract infections

- urinary tract infections

POLKA-200 Tablets

- OFLOXACIN 200 MG Packing: - 10X10 M.R.P: - 650PharmacodynamicsOfloxacin is a quinolone/fluoroquinolone antibiotic. Ofloxacin is bactericidal and its mode of action depends on blocking of bacterial DNA replication by binding itself to an enzyme called DNA gyrase

- which allows the untwisting required to replicate one DNA double helix into two. Notably the drug has 100 times higher affinity for bacterial DNA gyrase than for mammalian. Ofloxacin is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria. Mechanism of actionOfloxacin acts on DNA gyrase and toposiomerase IV

- enzymes which

- like human topoisomerase

POLKA-OZ Tablets

- OFLOXACIN 200mg

- ORNIDAZOLE 500mg

RION 625-LB Tablets

- AMOXICILLIN 200 MG & POTASSIUM CLAVULANATE 28.5 MG WITH LACTIC ACID BACILLUS Packing:- 1X10 M.R.P: - 260PHARMACOLOGY PHARMACOKINETICS: ABSORPTION: Dosing in the fasted or fed state has minimal effect on the pharmacokinetics of amoxicillin. While amoxicillin/clavulanate potassium can be given without regard to meals

- absorption of clavulanate potassium when taken with food is greater relative to the fasted state. In one study

- the relative bioavailability of clavulanate was reduced when amoxicillin/clavulanate potassium was dosed after eating something.DISTRIBUTION: Component in amoxicillin/clavulanate potassium is highly protein-bound; clavulanic acid is approximately 25% bound to human serum and amoxicillin approximately 18% bound. Amoxicillin diffuses readily into most body tissues and fluids with the exception of the brain and spinal fluid. METABOLISM AND EXCRETION: The half-life of amoxicillin after the oral administration of amoxicillin/clavulanate potassium is 1.3 hours and that of clavulanic acid is 1 hour. Approximately 50% to 70% of the amoxicillin and approximately 25% to 40% of the clavulanic acid are excreted unchanged in urine during the first 6 hours after administration of a single 250 mg/125 mg or 500 mg/125 mg tablet of amoxicillin/clavulanate potassium. INDICATIONS: Amoxicillin/clavulanic acid is a penicillin-type antibiotic used to treat a wide variety of bacterial infections. It works by stopping the growth of bacteria. This antibiotic only treats bacterial infections. It will not work for viral infections (e.g.

- common cold

RION-625 Tablets

- AMOXYCILLIN 500 MG & CLAVUNANIC ACID 125 MG Packing: - 1X10 M.R.P: -169PHARMACOLOGY PHARMACOKINETICS: ABSORPTION: Dosing in the fasted or fed state has minimal effect on the pharmacokinetics of amoxicillin. While amoxicillin/clavulanate potassium can be given without regard to meals

- absorption of clavulanate potassium when taken with food is greater relative to the fasted state. In one study

- the relative bioavailability of clavulanate was reduced when amoxicillin/clavulanate potassium was dosed after eating something. DISTRIBUTION: Component in amoxicillin/clavulanate potassium is highly protein-bound; clavulanic acid is approximately 25% bound to human serum and amoxicillin approximately 18% bound. Amoxicillin diffuses readily into most body tissues and fluids with the exception of the brain and spinal fluid. METABOLISM AND EXCRETION: The half-life of amoxicillin after the oral administration of amoxicillin/clavulanate potassium is 1.3 hours and that of clavulanic acid is 1 hour. Approximately 50% to 70% of the amoxicillin and approximately 25% to 40% of the clavulanic acid are excreted unchanged in urine during the first 6 hours after administration of a single 250 mg/125 mg or 500 mg/125 mg tablet of amoxicillin/clavulanate potassium. INDICATIONS: Amoxicillin/clavulanic acid is a penicillin-type antibiotic used to treat a wide variety of bacterial infections. It works by stopping the growth of bacteria. This antibiotic only treats bacterial infections. It will not work for viral infections (e.g.

- common cold

SIGTRAM-P Tablets

- TRAMADOL HCL37.5mg

- PCM 325mg

SPADSSPAS Tablets

- DROTAVERINE 80mg

- MEFENAMIC ACID 250mgPACKING: - 10X10 M.R.P: - 750Drotaverine Drotaverine is an effective spasmolytic drug. Mechanism of Action of Drotaverine Drotaverine has spasmolytic and vasodilating action. It exerts its action by inhibiting phosphodiesterase enzyme IV. This will leads to a decrease in cyclic AMP level and reduction in calcium ions (Ca2+). The reduction of calcium ions will dilates the unstipped muscles and blood vessels strongly and relieves spasm of smooth muscles.Pharmacokinets of Drotaverine Absorption: Drotaverine is rapidly absorbed after oral administration. Distribution: It is widely distributed in protein bound form. Metabolism: Extensively metabolised in the liver. Excretion: It is excreted mainly with the bile.Onset of Action for Drotaverine: -30 minutes Duration of Action for Drotaverine : -4 hours. Half Life of Drotaverine: -7 - 12 hours Mechanism of Action of Mefenamic Acid: - Mefenamic acid has analgesic

- anti-inflammatory and antipyretic action. It acts by inhibiting Prostaglandin (PGs) synthesis and their release at the site of injury. Prostaglandins cause tenderness and amplify the action of other analgesics. Mefenamic acid inhibits cyclo-oxygenase enzyme and antagonizes prostaglandin actions. Pharmacokinets of Mefenamic Acid Absorption: Mefenamic acid is well absorbed after oral administration. Distribution: It is distributed in the body in protein bound form. Metabolism: It is metabolised in the liver. Excretion: Mefenamic acid and its metabolites are excreted mainly in the urine.Onset of Action for Mefenamic Acid: - 1-2 hours. Duration of Action for Mefenamic Acid: -6 hours. Half Life of Mefenamic Acid: -2-4 hours

UXONOL-40 Tablets

- FEBUXOSTAT 40mg

WYTHAR-250 Tablets

- AZITHROMYCIN 250mg

WYTHAR-500 Tablets

- AZITHROMYCIN 500mg

XYLID-P Tablets

- NIMESULIDE 100mg

- PARACETAMOL 325mg

ZEED-6 Tablets

- DEFLAZACORT 6mg

ZIMFE-200 Tablets

- ACECLOFENAC 200mg

ZIMFE- MR Tablets

- ACECLOFENAC 100mg

- PCM 325mg

- CHLORZOXAZONE 250mg

ZIMFE-P Tablets

- ACECLOFENAC 100mg

- PCM 325mg

ZIMFE-SP Tablets

- ACECLOFENAC 100mg

- PCM 325mg

- SERRATIOPEPTIDASE 15mg