United States · FDA National Drug Code directory

NALTREXONE HYDROCHLORIDE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 70518-2718_57ad6bc6-2829-afb2-e063-6394a90a9da4
Product NDC: 70518-2718
Form: TABLET, FILM COATED
Composition / generic term: NALTREXONE HYDROCHLORIDE
Labeler: REMEDYREPACK INC.
Marketing category: ANDA
Marketing start / end (source format): 20200501
Source listing expiry: 20271231

Source-listed ingredients

NALTREXONE HYDROCHLORIDE — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2718-0) · 70518-2718-0

Source and coverage

Open FDA National Drug Code directory →

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →