Package 0615-8579-39

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-8579-39
Digits Only 0615857939
Product NDC 0615-8579
Product ID 0615-8579_cdb406b8-353a-42e0-be3d-076d2d789ddc
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8579-39)

Marketing

Marketing Status
Marketed Since 2025-08-27
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": "cdb406b8-353a-42e0-be3d-076d2d789ddc", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["fa2f842f-001a-4f1e-8748-c7852579109c"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8579-39)", "package_ndc": "0615-8579-39", "marketing_start_date": "20250827"}], "brand_name": "NALTREXONE HYDROCHLORIDE", "product_id": "0615-8579_cdb406b8-353a-42e0-be3d-076d2d789ddc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0615-8579", "generic_name": "NALTREXONE HYDROCHLORIDE", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALTREXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALTREXONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA090356", "marketing_category": "ANDA", "marketing_start_date": "20120229", "listing_expiration_date": "20261231"}