Package 63629-1046-1

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1046-1
Digits Only 6362910461
Product NDC 63629-1046
Product ID 63629-1046_98bc3962-2a5f-4014-abf8-22e415bbcb21
Description

30 TABLET, FILM COATED in 1 BOTTLE (63629-1046-1)

Marketing

Marketing Status
Marketed Since 2019-07-01
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": "98bc3962-2a5f-4014-abf8-22e415bbcb21", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["94c3e2de-36e4-42d4-b6e8-53b4aff1c4ed"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63629-1046-1)", "package_ndc": "63629-1046-1", "marketing_start_date": "20190701"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "63629-1046_98bc3962-2a5f-4014-abf8-22e415bbcb21", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "63629-1046", "generic_name": "Naltrexone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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": "20130923", "listing_expiration_date": "20261231"}