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ketorolac tromethamine 10 mg

INDICATIONS AND USAGE Carefully consider the potential benefits and risks of ketorolac tromethamine tablets and other treatment options before deciding to use ketorolac tromethamine tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals. Acute Pain in Adult Patients Ketorolac tromethamine tablets are indicated for the short-term (≀ 5 days) management of moderately severe acute pain that requires analgesia at the opioid level, usually in a postoperative setting. Therapy should always be initiated with intravenous or intramuscular dosing of ketorolac tromethamine, and ketorolac tromethamine tablets are to be used only as continuation treatment, if necessary. The total combined duration of use of ketorolac tromethamine tablets and ketorolac tromethamine is not to exceed 5 days of use because of the potential of increasing the frequency and severity of adverse reactions associated with the recommended doses (see WARNINGS , PRECAUTIONS , DOSAGE AND ADMINISTRATION , and ADVERSE REACTIONS ). Patients should be switched to alternative analgesics as soon as possible, but ketorolac tromethamine tablets therapy is not to exceed 5 days.

bionpharma inc.


2 months ago ROUND WHITE KT ketorolac tromethamine 10 mg

ROUND WHITE KT

2 months ago ROUND WHITE KT ketorolac tromethamine 10 mg

KT ROUND WHITE

HOW SUPPLIED

KETOROLAC TROMETHAMINE tablets, USP 10 mg are round, white, convex, unscored, film‑coated tablets, debossed “ KT ” on one side and plain on the other side, available in bottles of 100 tablets (NDC 69452-275-20). Storage Store at 20Âș to 25ÂșC (68Âș to 77ÂșF); excursions permitted to 15° to 30°C (59° to 86°F) [See USP Controlled Room Temperature]. Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required). PROTECT FROM LIGHT AND EXCESSIVE HUMIDITY. KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN. Distributed by: Bionpharma Inc. Princeton, NJ 08540 MADE IN INDIA Rev. 01/2023 FDA-05


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