Naltrexone Hydrochloride 68084-0291-21

Package NDC

68084-0291-21

Manufacturer: American Health Packaging
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 3, 2013
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

68084-0291-21Selected

30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-291-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-291-11)