Naltrexone Hydrochloride 67046-0306-03

Package NDC

67046-0306-03

Manufacturer: Coupler Llc
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 15, 2026
Listing Expires: December 31, 2027
Application: ANDA090356

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Active Ingredients

Ingredient	Strength
Naltrexone Hydrochloride	50 mg/1

Drug Class

Opioid Antagonist [EPC]Opioid Antagonists [MoA]

Selected Package

67046-0306-03Selected

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-0306-3)