Package 71335-2987-1

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2987-1
Digits Only 7133529871
Product NDC 71335-2987
Product ID 71335-2987_271632c9-1ca1-40e0-a003-f5c0408c7e57
Description

30 TABLET, FILM COATED in 1 BOTTLE (71335-2987-1)

Marketing

Marketing Status
Marketed Since 2025-11-10
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": "271632c9-1ca1-40e0-a003-f5c0408c7e57", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["ab5b3829-96e5-4123-967a-29b41f13a4f7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2987-1)", "package_ndc": "71335-2987-1", "marketing_start_date": "20251110"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "71335-2987_271632c9-1ca1-40e0-a003-f5c0408c7e57", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71335-2987", "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": "20240215", "listing_expiration_date": "20261231"}