Package 68084-291-21

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68084-291-21
Digits Only 6808429121
Product NDC 68084-291
Product ID 68084-291_1ef27c71-786e-4f5e-e063-6294a90a7934
Description

30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-291-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-291-11)

Marketing

Marketing Status
Marketed Since 2013-06-03
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": "1ef27c71-786e-4f5e-e063-6294a90a7934", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["81e25c6a-81b6-4cfb-91bf-be20c3ae546b"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-291-21)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-291-11)", "package_ndc": "68084-291-21", "marketing_start_date": "20130603"}], "brand_name": "NALTREXONE HYDROCHLORIDE", "product_id": "68084-291_1ef27c71-786e-4f5e-e063-6294a90a7934", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "68084-291", "generic_name": "naltrexone hydrochloride", "labeler_name": "American Health Packaging", "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": "20130603", "listing_expiration_date": "20261231"}