43 Products

- CEFOPERAZONE 1000MG + TAZOBACTAM 125MG

- CEFOPERAZONE 1000MG + SULBACTAM 500MG

- CEFOPERAZONE 500MG + SULBACTAM 500MG

- CEFEPIME 1000MG +TAZOBACTAM 125MG

- CEFIXIME 200MG + OFLOXACIN 200MG

- VANCOMYCIN 500MG

- VANCOMYCIN 1GM

- TESTOSTERONE ENANTHATE 250MG

- PIPERACILLIN 4GM + TAZOBACTAM 500MG

- PIPERACILLIN 4GM + TAZOBACTAM 500MG

- PIPERACILLIN 2000MG + TAZOBACTAM 250 MG

- IRON SUCROSE 100MG

- EDARAVONE 1.5MG

- PIROXICAM

- ARTESUNATE 120MG

- ARTESUNATE 60MG

- ESOMEPRAZOLE 40MG

- MEROPENEM 1GM+SULBATCUM 500MG INJECTION

- MEROPENEM-250MG

- MEROPENEM-125MG

- MEROPENEM-1GM

- LEVETIRACETAM AMPOULE 100MG/ML

- ESOMEPRAZOLE 40MG

- RABEPRAZOLE SODIUM Injection RABEPRAZOLE Rabeprazole 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

- ONDANSETRON 4mg PHARMACOLOGY 1. Pharmacokinetics: - Absorption: Owing to hepatic first-pass metabolism

- its bioavailability is only about 60%. Distribution: Plasma protein binding of ondensetron 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: Ondensetron 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

- COMPOSITION: - IRON SUCROSE 20 MG PACKING: - 5 ML M.R.P: - 179   I-BAR S injection (iron sucrose injection 20 mg) is an iron replacement product suggested for the treatment of iron deficiency anemia in patients with chronic kidney disease. Iron sucrose is a form of the mineral iron. Iron is important for many functions in the body

- especially for the transport of oxygen in the blood. Iron sucrose injection is used to treat iron deficiency anemia in people with kidney disease. It is usually given with another medication to promote the growth of red blood cells Pharmacology Iron sucrose is dissociated by the reticuloendothelial system into iron and sucrose. The released iron increases serum iron concentrations and is incorporated into hemoglobin. Distribution: - Vdss: Healthy adults: 7.9 L Metabolism: - Dissociated into iron and sucrose by the reticuloendothelial system Excretion: -Healthy adults: Urine (5%) within 24 hours Half-Life Elimination: - Healthy adults: 6 hours; Nondialysis-dependent adolescents: 8 hours

- NANDROLONE DECANOATE 25 MG Packing: -1 ML M.R.P: - 82   1. Hypogonadism: Testosterone is given for 2-3 years or until adequate sexual maturation takes place. 2. Cytorchidism : Human chorionic gonadotrophin treatment for 6 weeks of testosterone administration helps in testicular descent. 3. Androgens also enhance libido

- sexual performance

- and stimulate spermatogenesis. However

- the use of androgens in inpotency has to be based on properassessment of endocrine deficicncy as a cause of impotency. 4. Androgens are used with verying success in premenopausal breast carcinoma in famales. 5. Androgens have also been used to treat refractory anaemias and in selected cases of osteoporosis along with oestrogens.

- MEYHYLCOBALAMINE 1000mcg

- PYRIDOXINE 100mg

- NICOTINAMIDE 10mg

- MECOBALAMIN 250 mcg

- FOLIC ACID

- NIACINAMIDE & VITAMIN C 150 mg Packing: - COMBI PACK M.R.P: - 42   Methylcobalamin is a cobalamin (MeB12) used in peripheral neuropathy

- diabetic neuropathy etc. It is a form of vitamin B12. This vitamer is one of two active coenzymes used by B-12 dependent enzymes in the body

- CEFOPERAZONE 1000mg

- SULBACTUM 500mg

- PIPERACILLIN 4gm

- TAZOBACTUM 0.5gm Packing: - Vial M.R.P: - 427   Fixed 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.

- CEFTRIAXONE 1000mg

- CEFTRIAXONE 1000mg

- SULBACTUM 500mg

- CEFTRIAXONE 1000mg

- TAZOBACTUM 125mg

- AMIKACIN 250mg

- AMIKACIN 500mg

- (NANDROLONE DECANOATE 50 MG)   Full Description : C18 steroid with androgenic and anabolic properties. It is generally prepared from alkyl ethers of estradiol to resemble testosterone but less one carbon at the 19 position. This compound belongs to the class of organic compounds known as steroid esters. These are compounds containing a steroid moiety which bears a carboxylic acid ester group. PHARMACOLOGY PHARMACODYNAMICS: Nandrolone is an anabolic steroid occurring naturally in the human body

- albeit in small quantities. Nandrolone increases production and urinary excretion of erythropoietin. It may also have a direct action on bone marrow. Nandrolone binds to the androgen receptor to a greater degree than testosterone

- but due to its inability to act on the muscle in ways unmediated by the receptor

- has less overall effect on muscle growth. Nandrolone is an androgen receptor agonist. The drug bound to the receptor complexes which allows it to enter the nucleus and bind directly to specific nucleotide sequences of the chromosomal DNA. The areas of binding are called hormone response elements (HREs)

- (DICLOFENAC SODIUM INJ(1ML)   Pharmacology Pharmacokinetics Diclofenac Sodium • Absorption: – Diclofenac is NSAID with anti-inflammatory

- analgesic and antipyretic properties. It is rapidly and almost completely absorbed when administered as an oral dose. Food does not have a significant effect on the extent of oral absorption. • Protein Binding: -At therapeutic concentrations

- it is more than 99% bound to plasma proteins. Metabolism: -Diclofenac and/or its metabolites are rapidly and preferentially taken up and retained in inflamed tissues. It penetrates synovial fluid where concentrations may persist even when plasma concentrations fall. • Half-Life: – The terminal half-life is about 1 to 2 hours. Diclofenac acts by inhibiting cyclooxygenase

- thus prevents the formation of prostaglandins

- (PANTOPRAZOLE INJ)   Pharmacology Pharmacodynamics: – Pantoprazole act by selectively inhibiting the H+/K+ – ATPase enzyme in the secretory canaliculus of the stimulated parietal cell. Within this cell

- the function of the enzyme is to secrete acid by forcing an exchange of H3O+ for K+ when a K+ -Cl- pathway is parallel to the pump. The result of pump turnover is the secretion of HCl into the stomach. This is the final common pathway for acid secretion. Pump inhibition blocks acid secretion regardless of whether it originates from stimulation of muscarinic

- gastrin

- or histamine receptors Pharmacokinetics: – • Absorption and Distribution: – Following intravenous administration of pantoprazole

- PROGESTERONE 200 MG   The Corpus luteum and placenta secretes progestational which is a major steroid. The main function of progesterone is to function on the uterus

- the mammary glands

- and the brain. The other functions of progesterone are to maintain the pregnancy

- mammary tissue development to produce milk. PROGESTERONE IS A FEMALE HORMONE ESSENTIAL FOR THE REGULATION OF OVULATION AND MENSTRUATION. PHARMACOLOGY a.) Pharmacodynamics: A naturally occurring hormone which is a female sex hormone. To understand the pharmacodynamics of progesterone is important to know about the process of a woman’s normal menstrual cycle

- (AMOXYCILLIN 1 GM & CLAVULANATE 200 MG)

- (MEROPENEM 1 GM)   Meropenem is a broad-spectrum carbapenem antibiotic. It is active against Gram-positive and Gram-negative bacteria. Meropenem exerts its action by penetrating bacterial cells readily and interfering with the synthesis of vital cell wall components

- which leads to cell death. PHARMACOLOGY PHARMACODYNAMICS: – The bactericidal activity of meropenem results from the inhibition of cell wall synthesis. Meropenem readily penetrates the cell wall of most Gram-positive and Gram-negative bacteria to reach penicillin-binding- protein (PBP) targets. Its strongest affinities are toward PBPs 2

- 3 and 4 of Escherichia coli and Pseudomonas aeruginosa; and PBPs 1

- 2 and 4 of Staphylococcus aureus. PHARMACOKINETICS: – • ROUTE OF ELIMINATION: – Approximately 70% of the intravenously administered dose is recovered as unchanged meropenem in the urine over 12 hours

- TRIAMCINOLONE 40MG