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NDC 68094-0909-30

Naltrexone Hydrochloride 50 mg/1 TABLET, FILM COATED

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NDC
68094-0909-30
Generic Name
Naltrexone Hydrochloride
Brand Name
Naltrexone Hydrochloride
Strength
50 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Package Size
Labeler
Precision Dose Inc.

FDA Drug Information

Indications & Usage

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.

Important Warnings

WARNINGS Vulnerability to Opioid Overdose After opioid detoxification, patients are likely to have reduced tolerance to opioids. As the blockade of exogenous opioids provided by naltrexone hydrochloride wanes and eventually dissipates completely, patients who have been treated with naltrexone hydrochloride may respond to lower doses of opioids than previously used, just as they would shortly after…

Source: FDA. For professional use only. Not a substitute for prescribing information.

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