Package 0406-1170-01

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0406-1170-01
Digits Only 0406117001
Product NDC 0406-1170
Product ID 0406-1170_9ed13551-325e-4b82-a266-72fc89ed27dc
Description

100 TABLET, FILM COATED in 1 BOTTLE (0406-1170-01)

Marketing

Marketing Status
Marketed Since 2002-03-22
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": "9ed13551-325e-4b82-a266-72fc89ed27dc", "openfda": {"upc": ["0304061170017"], "unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["06ff2d5a-e62b-4fa4-bbdb-01938535bc65"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0406-1170-01)", "package_ndc": "0406-1170-01", "marketing_start_date": "20020322"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0406-1170-03)", "package_ndc": "0406-1170-03", "marketing_start_date": "20020322"}], "brand_name": "NALTREXONE HYDROCHLORIDE", "product_id": "0406-1170_9ed13551-325e-4b82-a266-72fc89ed27dc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0406-1170", "generic_name": "naltrexone hydrochloride", "labeler_name": "SpecGx LLC", "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"}