Package 68071-3654-3

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3654-3
Digits Only 6807136543
Product NDC 68071-3654
Product ID 68071-3654_2a2ff668-e2bb-5308-e063-6294a90a832d
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-3654-3)

Marketing

Marketing Status
Marketed Since 2024-07-24
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": "2a2ff668-e2bb-5308-e063-6294a90a832d", "openfda": {"upc": ["0368071365436"], "unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["1e059495-5e64-0cb0-e063-6394a90a3ffc"], "manufacturer_name": ["NuCare Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3654-3)", "package_ndc": "68071-3654-3", "marketing_start_date": "20240724"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "68071-3654_2a2ff668-e2bb-5308-e063-6294a90a832d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "68071-3654", "generic_name": "Naltrexone Hydrochloride", "labeler_name": "NuCare Pharmaceuticals Inc.", "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"}