NDC 71610-919 – Naltrexone Hydrochloride

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

Human Prescription Drug

Product NDC71610-919

Product details

Brand name
Naltrexone Hydrochloride
Generic name
Naltrexone hydrochloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
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 (1)

Package NDCDescriptionSince
71610-919-31600 TABLET, FILM COATED in 1 BOTTLE (71610-919-31)Jul 1, 2025

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