NDC 42291-632 – Naltrexone Hydrochloride

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

Human Prescription Drug

Product NDC42291-632

Product details

Brand name
Naltrexone Hydrochloride
Generic name
Naltrexone Hydrochloride
Labeler
AvKARE
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075274
Marketed since
March 26, 2015
Marketing end
June 30, 2028
Pharmacologic class
Opioid Antagonist

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
42291-632-3030 TABLET, FILM COATED in 1 BOTTLE (42291-632-30)Mar 26, 2015
42291-632-6060 TABLET, FILM COATED in 1 BOTTLE (42291-632-60)Jul 24, 2025

Other Naltrexone Hydrochloride products