30 Products

in Antibiotics

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

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

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

WYTHAR-250 Tablets

- AZITHROMYCIN 250mg

WYTHAR-500 Tablets

- AZITHROMYCIN 500mg

SIGBECT-S 1.5GM

- CEFOPERAZONE 1000mg

- SULBACTUM 500mg

SIGTAZO Injection

- PIPERACILLIN 4gm

- TAZOBACTUM 0.5gmPacking: - Vial M.R.P: - 427Fixed combination of Piperacillin sodium ( an extended spectrum penicillin) & tazobactam sodium ( a B-lactamase inhibitor).Tazobactum synergistically expands piperacilin’s spectrum of activity aginst B-lactamase-producing bacteria by irreversibly & completely inhibiting B-lactamase. Spectrum of activity includes many gram-positive and gram-negative aerobes and some anaerobes. EFFECTIVE Intensive care medicine ( pneumonia

- peritonitis) Diabetes-related foot infections Gyneocologic & obstetric infections Intra-abdominal infections. Respiratory tract infections. Septicemia Febrile neutropenia skin & skin structure infections urinary tract infections.

ULFAZ 1gm Injection

- CEFTRIAXONE 1000mg

ULFAZ-S 1.5gm Injection

- CEFTRIAXONE 1000mg

- SULBACTUM 500mg

ULFAZ-T Injection

- CEFTRIAXONE 1000mg

- TAZOBACTUM 125mg

ZYMIK-250 Injection

- AMIKACIN 250mg

ZYMIK-500 Injection

- AMIKACIN 500mg

FAXLI-OZ Suspension

- LEVOFLOXACIN 125mg

- ORNIDAZOLE 125mgPHARMACODYNAMICS: - Levofloxacin

- a fluoroquinolone antiinfective

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

FYCEF Dry Syrup

- 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

PODZY-50 Suspension

- CEFPODOXIME 50 ORAL SUSPENSION Packing: - 30 MLM.R.P:- 65Pharmacology Absorption and Excretion: Cefpodoxime Proxetil is a prodrug that is absorbed from the gastrointestinal tract and de-esterified to its active metabolite

- cefpodoxime. The oral administration of 100 mg of Cefpodoxime Proxetil to fasting subjects

- approximately 50% of the administered cefpodoxime dose was absorbed systemically. Over the recommended dosing range (100 to 400 mg)

- approximately 29 to 33% of the administered cefpodoxime dose was excreted unchanged in the urine in 12 hours. There is minimal metabolism of cefpodoxime in vivo. Pharmacokinetics of Cefpodoxime Over the recommended dosing range

PODZY-100 Dry Syrup

- CEFPODOXIME 100MG Packing: - 30 ML M.R.P: -115Pharmacology Absorption and Excretion: Cefpodoxime Proxetil is a prodrug that is absorbed from the gastrointestinal tract and de-esterified to its active metabolite

- cefpodoxime. The oral administration of 100 mg of Cefpodoxime Proxetil to fasting subjects

- approximately 50% of the administered cefpodoxime dose was absorbed systemically. Over the recommended dosing range (100 to 400 mg)

- approximately 29 to 33% of the administered cefpodoxime dose was excreted unchanged in the urine in 12 hours. There is minimal metabolism of cefpodoxime in vivo. Pharmacokinetics of Cefpodoxime Over the recommended dosing range

POLKA Suspension

- OFLOXACIN 50 mg Packing: - 60Ml M.R.P: -39Pharmacodynamics: -Ofloxacin 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 action:- Ofloxacin acts on DNA gyrase and toposiomerase IV

- enzymes which

- like human topoisomerase

RION Dry Syrup

- AMOXYCILLIN 200 MG & CLAVULANATE POTASSIUM 28.5 MG Packing: - 30ML M.R.P:- 52PHARMACOLOGY 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