Package 71335-3039-1

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-3039-1
Digits Only 7133530391
Product NDC 71335-3039
Product ID 71335-3039_390e2929-b886-4f85-9b7f-1758a5783e26
Description

30 TABLET, FILM COATED in 1 BOTTLE (71335-3039-1)

Marketing

Marketing Status
Marketed Since 2025-12-03
Brand naltrexone hydrochloride
Generic naltrexone hydrochloride
Sample Package No

Linked Drug Pages (1)

Naltrexone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "390e2929-b886-4f85-9b7f-1758a5783e26", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["d4d0537b-113a-4e49-bb50-bf5ddafe6b7d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-3039-1)", "package_ndc": "71335-3039-1", "marketing_start_date": "20251203"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "71335-3039_390e2929-b886-4f85-9b7f-1758a5783e26", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71335-3039", "generic_name": "Naltrexone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naltrexone Hydrochloride", "active_ingredients": [{"name": "NALTREXONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA075274", "marketing_category": "ANDA", "marketing_start_date": "20250815", "listing_expiration_date": "20261231"}