Package 71335-3011-1

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-3011-1
Digits Only 7133530111
Product NDC 71335-3011
Product ID 71335-3011_0cc8b23f-4ee7-47f8-b2d6-b752392c6f14
Description

30 TABLET, FILM COATED in 1 BOTTLE (71335-3011-1)

Marketing

Marketing Status
Marketed Since 2025-11-18
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": "0cc8b23f-4ee7-47f8-b2d6-b752392c6f14", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["8f019ac1-13a8-42f2-bdb2-8aaef5896d96"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-3011-1)", "package_ndc": "71335-3011-1", "marketing_start_date": "20251118"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "71335-3011_0cc8b23f-4ee7-47f8-b2d6-b752392c6f14", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71335-3011", "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"}