Package 0406-5755-62

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0406-5755-62
Digits Only 0406575562
Product NDC 0406-5755
Description

100 TABLET in 1 BLISTER PACK (0406-5755-62)

Marketing

Marketing Status
Marketed Since 2004-04-27
Brand methadone hydrochloride
Generic methadone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "72ab3c44-1cd7-41e9-8b6a-e030fdf65bc2", "openfda": {"upc": ["0304065755012", "0304065771012"], "unii": ["229809935B"], "rxcui": ["864706", "864718"], "spl_set_id": ["eddf7077-02fb-4771-9823-31984f4ff2bb"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0406-5755-01)", "package_ndc": "0406-5755-01", "marketing_start_date": "20040427"}, {"sample": false, "description": "1 TABLET in 1 BLISTER PACK (0406-5755-23)", "package_ndc": "0406-5755-23", "marketing_start_date": "20040427"}, {"sample": false, "description": "100 TABLET in 1 BLISTER PACK (0406-5755-62)", "package_ndc": "0406-5755-62", "marketing_start_date": "20040427"}], "brand_name": "METHADONE HYDROCHLORIDE", "product_id": "0406-5755_72ab3c44-1cd7-41e9-8b6a-e030fdf65bc2", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0406-5755", "dea_schedule": "CII", "generic_name": "METHADONE HYDROCHLORIDE", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHADONE HYDROCHLORIDE", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA040517", "marketing_category": "ANDA", "marketing_start_date": "20040427", "listing_expiration_date": "20261231"}