Naltrexone Hydrochloride 16729-0081-10

Package NDC

16729-0081-10

Manufacturer: Accord Healthcare, Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 18, 2012
Listing Expires: December 31, 2026
Application: ANDA091205

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Active Ingredients

Ingredient	Strength
Naltrexone Hydrochloride	50 mg/1

Drug Class

Opioid Antagonist [EPC]Opioid Antagonists [MoA]

Selected Package

16729-0081-10Selected

30 TABLET, FILM COATED in 1 BOTTLE (16729-081-10)

Other packages for this product(1)

16729-0081-01

100 TABLET, FILM COATED in 1 BOTTLE (16729-081-01)

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