Package 50090-4925-0

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-4925-0
Digits Only 5009049250
Product NDC 50090-4925
Product ID 50090-4925_4242e317-1764-436a-aff6-338a58f1b0a2
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-4925-0)

Marketing

Marketing Status
Marketed Since 2020-02-20
Brand naltrexone hydrochloride
Generic naltrexone hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4242e317-1764-436a-aff6-338a58f1b0a2", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["00c04ff4-b6f2-466c-9ab9-813a60577db0"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-4925-0)", "package_ndc": "50090-4925-0", "marketing_start_date": "20200220"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "50090-4925_4242e317-1764-436a-aff6-338a58f1b0a2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "50090-4925", "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": "ANDA091205", "marketing_category": "ANDA", "marketing_start_date": "20120118", "listing_expiration_date": "20261231"}