NDC 70518-4344 – Naltrexone Hydrochloride

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

Human Prescription Drug

Product NDC70518-4344

Product details

Brand name
Naltrexone Hydrochloride
Generic name
Naltrexone Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075274
Marketed since
May 20, 2025
Marketing end
November 30, 2027
Pharmacologic class
Opioid Antagonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
70518-4344-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-4344-0)May 20, 2025

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