NDC 71335-2062 – Naltrexone Hydrochloride

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

Human Prescription Drug

Product NDC71335-2062

Product details

Brand name
Naltrexone Hydrochloride
Generic name
Naltrexone Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090356
Marketed since
February 29, 2012
Listing expires
December 31, 2027
Pharmacologic class
Opioid Antagonist

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
71335-2062-130 TABLET, FILM COATED in 1 BOTTLE (71335-2062-1)Mar 21, 2022
71335-2062-290 TABLET, FILM COATED in 1 BOTTLE (71335-2062-2)Mar 21, 2022
71335-2062-360 TABLET, FILM COATED in 1 BOTTLE (71335-2062-3)Mar 21, 2022
71335-2062-445 TABLET, FILM COATED in 1 BOTTLE (71335-2062-4)Mar 21, 2022
71335-2062-5120 TABLET, FILM COATED in 1 BOTTLE (71335-2062-5)Mar 21, 2022
71335-2062-615 TABLET, FILM COATED in 1 BOTTLE (71335-2062-6)Mar 21, 2022
71335-2062-7100 TABLET, FILM COATED in 1 BOTTLE (71335-2062-7)Mar 21, 2022

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