Tanzanija - anglų - Tanzania Medicinces & Medical Devices Authority

sun pharmaceutical industries limited, india - divalproex sodium - tablets - 500 mg

Tanzanija - anglų - Tanzania Medicinces & Medical Devices Authority

sun pharmaceutical industries limited, india - divalproex sodium - tablets - 250 mg

Australija - anglų - Department of Health (Therapeutic Goods Administration)

sun pharmaceuticals industries australia pty ltd - octreotide -

Australija - anglų - Department of Health (Therapeutic Goods Administration)

sun pharmaceuticals industries australia pty ltd - oxaliplatin -

Australija - anglų - Department of Health (Therapeutic Goods Administration)

sun pharmaceuticals industries australia pty ltd - pantoprazole sodium -

Airija - anglų - HPRA (Health Products Regulatory Authority)

sun pharmaceutical industries europe b.v. - warfarin sodium clathrate - tablet - 2.5 milligram(s) - vitamin k antagonists; warfarin - antithrombotic agent (vitamin k antagonist) - it is indicated for the prophylaxis of venous thrombosis and pulmonary embolism, and for use in the treatment of these conditions to prevent their extension and for the prophylaxis of systemic embolisation in patients with rheumatic heart disease and atrial fibrillation.

Jungtinės Valstijos - anglų - NLM (National Library of Medicine)

sun pharmaceutical industries, inc. - acetaminophen (unii: 362o9itl9d) (acetaminophen - unii:362o9itl9d), hydrocodone bitartrate (unii: no70w886kk) (hydrocodone - unii:6yks4y3wq7) - acetaminophen 325 mg - hydrocodone bitartrate and acetaminophen tablets, usp are indicated for the management of moderate to moderately severe pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate. limitations of use because of the risks of addiction, abuse, and misuse, with opioids, even at recommended doses [see warnings ], reserve hydrocodone bitartrate and acetaminophen tablets, usp for use in patients for whom alternative treatment options (e.g., non-opioid analgesics): hydrocodone bitartrate and acetaminophen tablets, usp are contraindicated in patients with:

Airija - anglų - HPRA (Health Products Regulatory Authority)

sun pharmaceutical industries europe b.v. - clarithromycin - film-coated tablet - 250 milligram(s) - macrolides; clarithromycin

Airija - anglų - HPRA (Health Products Regulatory Authority)

sun pharmaceutical industries europe b.v. - clarithromycin - film-coated tablet - 500 milligram(s) - macrolides; clarithromycin

Didžioji Britanija - anglų - MHRA (Medicines & Healthcare Products Regulatory Agency)

sun pharmaceutical industries europe b.v. - codeine phosphate - oral tablet - 30mg