Naltrexone Hydrochloride 70518-4344-00

Package NDC

70518-4344-00

Manufacturer: Remedyrepack Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: May 20, 2025
Listing Expires: December 31, 2026
Application: ANDA075274

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Active Ingredients

Ingredient	Strength
Naltrexone Hydrochloride	50 mg/1

Drug Class

Opioid Antagonist [EPC]Opioid Antagonists [MoA]

Selected Package

70518-4344-00Selected

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4344-0)