Package 70518-4344-0

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4344-0
Digits Only 7051843440
Product NDC 70518-4344
Product ID 70518-4344_4031031d-3b90-1644-e063-6294a90ae5a4
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4344-0)

Marketing

Marketing Status
Marketed Since 2025-05-20
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": "4031031d-3b90-1644-e063-6294a90ae5a4", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["db911559-26f5-43a0-b61f-3425176c936f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4344-0)", "package_ndc": "70518-4344-0", "marketing_start_date": "20250520"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "70518-4344_4031031d-3b90-1644-e063-6294a90ae5a4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "70518-4344", "generic_name": "Naltrexone Hydrochloride", "labeler_name": "REMEDYREPACK 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": "20250520", "listing_expiration_date": "20261231"}