Package 0054-0392-68

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0054-0392-68
Digits Only 0054039268
Product NDC 0054-0392
Description

1000 mL in 1 BOTTLE (0054-0392-68)

Marketing

Marketing Status
Marketed Since 2010-03-16
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": "2b59a769-5e79-4372-8dbd-3ae4e7d56d07", "openfda": {"upc": ["0300540391683", "0300540392680"], "unii": ["229809935B"], "rxcui": ["991147"], "spl_set_id": ["e72841bf-364b-49b1-8e69-7e26ddcd2657"], "manufacturer_name": ["Hikma Pharmaceuticals USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE (0054-0392-68)", "package_ndc": "0054-0392-68", "marketing_start_date": "20100316"}], "brand_name": "Methadone Hydrochloride", "product_id": "0054-0392_2b59a769-5e79-4372-8dbd-3ae4e7d56d07", "dosage_form": "CONCENTRATE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0054-0392", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA040180", "marketing_category": "ANDA", "marketing_start_date": "20100316", "listing_expiration_date": "20261231"}