NDC 51224-206

Naltrexone Hydrochloride 50 mg tablet, film coated

On the label: TAGI Pharma, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Elite Laboratories, Inc.Northvale, NJ, United StatesMakes it Problems found, fixed voluntarilyAug 1, 2025 · 12 inspections, 1 with FDA action

Product details

Generic drug
Naltrexone: every company that makes it
Form
tablet, film coated, oral
Strength
50 mg
Approval
ANDA ANDA075274
On the market since
Sep 23, 2013
Package NDCs
51224-206-30 51224-206-50
Official label
DailyMed (National Library of Medicine), updated Nov 18, 2025

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