NDC 71335-1480 – Naltrexone Hydrochloride

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

Human Prescription Drug

Product NDC71335-1480

Product details

Brand name
Naltrexone Hydrochloride
Generic name
Naltrexone hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076264
Marketed since
March 22, 2002
Listing expires
December 31, 2026
Pharmacologic class
Opioid Antagonist

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
71335-1480-130 TABLET, FILM COATED in 1 BOTTLE (71335-1480-1)Jan 16, 2020
71335-1480-290 TABLET, FILM COATED in 1 BOTTLE (71335-1480-2)Jan 22, 2020
71335-1480-360 TABLET, FILM COATED in 1 BOTTLE (71335-1480-3)May 30, 2024
71335-1480-445 TABLET, FILM COATED in 1 BOTTLE (71335-1480-4)May 30, 2024
71335-1480-5120 TABLET, FILM COATED in 1 BOTTLE (71335-1480-5)May 30, 2024
71335-1480-615 TABLET, FILM COATED in 1 BOTTLE (71335-1480-6)Sep 10, 2020

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