Package 50090-6820-0

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6820-0
Digits Only 5009068200
Product NDC 50090-6820
Product ID 50090-6820_074fe42c-ca67-4dda-8bc8-30a6c2cd1c4f
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-6820-0)

Marketing

Marketing Status
Marketed Since 2023-11-14
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": "074fe42c-ca67-4dda-8bc8-30a6c2cd1c4f", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["0103a32b-14a9-48a8-8952-b2b12ef09649"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6820-0)", "package_ndc": "50090-6820-0", "marketing_start_date": "20231114"}], "brand_name": "NALTREXONE HYDROCHLORIDE", "product_id": "50090-6820_074fe42c-ca67-4dda-8bc8-30a6c2cd1c4f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "50090-6820", "generic_name": "naltrexone hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALTREXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALTREXONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA076264", "marketing_category": "ANDA", "marketing_start_date": "20020322", "listing_expiration_date": "20261231"}