NOT APPLICABLE- omeprazole sodium bicarbonate capsule États-Unis - anglais - NLM (National Library of Medicine)

not applicable- omeprazole sodium bicarbonate capsule

sterling knight pharmaceuticals llc - omeprazole (unii: kg60484qx9) (omeprazole - unii:kg60484qx9), sodium bicarbonate (unii: 8mdf5v39qo) (sodium cation - unii:lyr4m0nh37) - omeprazole 40 mg - omeprazole and sodium bicarbonate is a proton pump inhibitor indicated for: - short-term treatment of active duodenal ulcer (1.1) - short-term treatment of active benign gastric ulcer (1.2) - treatment of gastroesophageal reflux disease (gerd) (1.3) - maintenance of healing of erosive esophagitis (1.4) the safety and effectiveness of omeprazole and sodium bicarbonate capsules in pediatric patients (<18 years of age) have not been established. (8.4) omeprazole and sodium bicarbonate is indicated for short-term treatment of active duodenal ulcer. most patients heal within four weeks. some patients may require an additional four weeks of therapy. [see clinical studies (14.1)] gastric ulcer omeprazole and sodium bicarbonate is indicated for short-term treatment (4-8 weeks) of active benign gastric ulcer. [see clinical studies (14.2)] symptomatic gerd omeprazole and sodium bicarbonate is indicated for the treatment of heartburn and other symptoms associated with gerd for up to 4 weeks. [see clinical studies (14.3)

CYCLOBENZAPRINE HYDROCHLORIDE capsule, film coated, extended release États-Unis - anglais - NLM (National Library of Medicine)

cyclobenzaprine hydrochloride capsule, film coated, extended release

sterling knight pharmaceuticals,llc - cyclobenzaprine hydrochloride (unii: 0ve05jys2p) (cyclobenzaprine - unii:69o5wqq5ti) - cyclobenzaprine hydrochloride 5 mg - cyclobenzaprine hydrochloride tablets, usp are indicated as an adjunct to rest and physical therapy for relief of muscle spasm associated with acute, painful musculoskeletal conditions. improvement is manifested by relief of muscle spasm and its associated signs and symptoms, namely, pain, tenderness, limitation of motion and restriction in activities of daily living. cyclobenzaprine hydrochloride tablets, usp should be used only for short periods (up to two or three weeks) because adequate evidence of effectiveness for more prolonged use is not available and because muscle spasm associated with acute, painful musculoskeletal conditions is generally of short duration and specific therapy for longer periods is seldom warranted. cyclobenzaprine hydrochloride tablets, usp have not been found effective in the treatment of spasticity associated with cerebral or spinal cord disease, or in children with cerebral palsy. hypersensitivity to any component of this product. concomitant use of monoamine oxidase (mao) inhi

OMNIVEX tablet États-Unis - anglais - NLM (National Library of Medicine)

omnivex tablet

sterling knight pharmaceuticals llc - ascorbic acid (unii: pq6ck8pd0r) (ascorbic acid - unii:pq6ck8pd0r), cholecalciferol (unii: 1c6v77qf41) (cholecalciferol - unii:1c6v77qf41), thiamine hydrochloride (unii: m572600e5p) (thiamine ion - unii:4abt0j945j), pyridoxal phosphate anhydrous (unii: f06sge49m6) (pyridoxal phosphate anhydrous - unii:f06sge49m6), folic acid (unii: 935e97boy8) (folic acid - unii:935e97boy8), methylcobalamin (unii: br1sn1js2w) (methylcobalamin - unii:br1sn1js2w), nadh (unii: 4j24dq0916) (nadh - unii:4j24dq0916), coenz - ascorbic acid 125 mg - omnivex is an orally administered prescription vitamin formulation for the clinical dietary management of suboptimal nutritional status in patients where advanced folate supplementation is required and nutritional supplementation in physiologically stressful conditions for maintenance of good health is needed. omnivex should be administered under the supervision of a licensed medical practitioner.

PRODIGEN- lactobacillus acidophilus capsule États-Unis - anglais - NLM (National Library of Medicine)

prodigen- lactobacillus acidophilus capsule

sterling knight pharmaceuticals llc - lactobacillus acidophilus (unii: 1prr1v42v5) (lactobacillus acidophilus - unii:1prr1v42v5), bifidobacterium animalis lactis (unii: 5307v7xw8i) (bifidobacterium animalis lactis - unii:5307v7xw8i) - prodigen is an orally administered prescription probiotic formulation for the clinical dietary management of suboptimal nutritional status in patients where advanced supplementation is required and nutritional supplementation in physiologically stressful conditions for maintenance of good health is needed. prodigen should be administered under the supervision of a licensed medical practitioner.

FENOPROFEN CALCIUM capsule États-Unis - anglais - NLM (National Library of Medicine)

fenoprofen calcium capsule

sterling knight pharmaceuticals - fenoprofen calcium (unii: 0x2cw1qabj) (fenoprofen - unii:ra33eac7ky) - fenoprofen 200 mg - fenoprofen calcium is indicated for: - relief of mild to moderate pain in adults. - relief of the signs and symptoms of rheumatoid arthrites. - relief of the signs and symptoms of osteoarthritis. fenoprofen calcium is contraindicated in the following patients: - known hypersensitivity (e.g., anaphylactic reactions and serious skin reactions) to fenoprofen or any components of the drug product [ see warnings and precautions (5.7, 5.9) ] - history of asthma, urticaria, or other allergic-type reactions after taking aspirin or other nsaids. severe, sometimes fatal, anaphylactic reactions to nsaids have been reported in such patients [ see warnings and precautions (5.7, 5.8) ] - in the setting of coronary artery bypass graft (cabg) surgery [ see warnings and precautions (5.1) ] risk summary use of nsaids, including fenoprofen calcium, during the third trimester of pregnancy increases the risk of premature closure of the fetal ductus arteriosus. avoid use of nsaids, including fenoprofen calcium, in pregnant w

Boston Scientific Sterling™ OTW PTA Balloon Dilatation Catheter Singapour - anglais - HSA (Health Sciences Authority)

boston scientific sterling™ otw pta balloon dilatation catheter

boston scientific asia pacific pte. ltd. - cardiovascular - the sterling otw pta balloon dilatation catheter is indicated for percutaneous transluminal angioplasty (pta) in the peripheral vasculature, including iliac, femoral, popliteal, infra-popliteal, and renal arteries, and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. this device is also indicated for post-dilatation of balloon expandable and self-expanding stents in the peripheral vasculature.

Boston Scientific Sterling™ SL Monorail™ PTA Balloon Dilatation Catheters Singapour - anglais - HSA (Health Sciences Authority)

boston scientific sterling™ sl monorail™ pta balloon dilatation catheters

boston scientific asia pacific pte. ltd. - cardiovascular - the sterling sl catheters are indicated for percutaneous transluminal angioplasty (pta) in the peripheral vasculature including iliac, femoral, ilio-femoral, infrapopliteal, popliteal, and renal arteries, and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae.

Boston Scientific Sterling™ SL Over-the-Wire PTA Balloon Dilatation Catheters Singapour - anglais - HSA (Health Sciences Authority)

boston scientific sterling™ sl over-the-wire pta balloon dilatation catheters

boston scientific asia pacific pte. ltd. - cardiovascular - the sterling sl catheters are indicated for percutaneous transluminal angioplasty (pta) in the peripheral vasculature including iliac, femoral, ilio-femoral, infrapopliteal, popliteal, and renal arteries, and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae.