NDC 71335-3012 – Naltrexone Hydrochloride

Naltrexone Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-3012

Product details

Brand name
Naltrexone Hydrochloride
Generic name
Naltrexone Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075274
Marketed since
August 15, 2025
Listing expires
December 31, 2026
Pharmacologic class
Opioid Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Naltrexone Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
71335-3012-1100 TABLET, FILM COATED in 1 BOTTLE (71335-3012-1)Nov 18, 2025

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