Naltrexone hydrochloride 50 MG Oral Tablet
INDICATIONS AND USAGE Naltrexone Hydrochloride Tablets USP are indicated in the treatment of alcohol dependence and for the blockade of the effects of exogenously administered opioids. Naltrexone Hydrochloride Tablets USP have not been shown to provide any therapeutic benefit except as part of an appropriate plan of management for the addictions.
precision dose inc.
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HOW SUPPLIED
NALTREXONE HYDROCHLORIDE Tablets, USP are available as: 50 mg; yellow, round film-coated tablets, bisected on one side, debossed with "EL" on one side of the bisect and "15" on the other side of the bisect. NDC 68094-853-62 Unit Dose Packages of 30 Tablets (3 × 10) per carton NDC 68094-853-61 Unit Dose Packages of 100 Tablets (10 × 10) per carton NDC 68094-853-66 Unit Dose Packages of 20 Tablets (2 × 10) per carton Store at 20° to 25°C (68° to 77°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. KEEP THIS AND ALL MEDICATIONS OUT DF THE REACH OF CHILDREN. These are not all the possible side effects of
NALTREXONE HYDROCHLORIDE Tablets, USP. Call your doctor for medical advice about side effects. You may report side effects to Precision Dose, Inc. at 1-800-397-9228 or to FDA at 1-800-FDA-1088. For more information go to dailymed.nlm.nih.gov.
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