Naltrexone Hydrochloride 71610-0919-31

Package NDC

71610-0919-31

Manufacturer: Aphena Pharma Solutions - Tennessee, Llc
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: March 22, 2002
Listing Expires: December 31, 2026
Application: ANDA076264

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Active Ingredients

Ingredient	Strength
Naltrexone Hydrochloride	50 mg/1

Drug Class

Opioid Antagonist [EPC]Opioid Antagonists [MoA]

Selected Package

71610-0919-31Selected

600 TABLET, FILM COATED in 1 BOTTLE (71610-919-31)