Naltrexone Hydrochloride 23155-0886-01

Package NDC

23155-0886-01

Manufacturer: Heritage Pharmaceuticals Inc D/b/a Avet Pharmaceuticals Inc
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: October 6, 2023
Listing Expires: December 31, 2026
Application: ANDA207905

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Active Ingredients

Ingredient	Strength
Naltrexone Hydrochloride	50 mg/1

Drug Class

Opioid Antagonist [EPC]Opioid Antagonists [MoA]

Selected Package

23155-0886-01Selected

100 TABLET, FILM COATED in 1 BOTTLE (23155-886-01)

Other packages for this product(1)

23155-0886-03

30 TABLET, FILM COATED in 1 BOTTLE (23155-886-03)

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