Package 82804-199-30

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-199-30
Digits Only 8280419930
Product NDC 82804-199
Product ID 82804-199_f3305f0b-fb9e-4009-b28f-47fe9b1b618b
Description

30 TABLET, FILM COATED in 1 BOTTLE (82804-199-30)

Marketing

Marketing Status
Marketed Since 2025-02-21
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": "f3305f0b-fb9e-4009-b28f-47fe9b1b618b", "openfda": {"upc": ["0382804199303"], "unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["f3305f0b-fb9e-4009-b28f-47fe9b1b618b"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (82804-199-30)", "package_ndc": "82804-199-30", "marketing_start_date": "20250221"}], "brand_name": "NALTREXONE HYDROCHLORIDE", "product_id": "82804-199_f3305f0b-fb9e-4009-b28f-47fe9b1b618b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "82804-199", "generic_name": "NALTREXONE HYDROCHLORIDE", "labeler_name": "Proficient Rx LP", "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"}