Package 66689-694-79

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 66689-694-79
Digits Only 6668969479
Product NDC 66689-694
Description

1000 mL in 1 BOTTLE (66689-694-79)

Marketing

Marketing Status
Marketed Since 2009-10-30
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": "a139d04a-25e0-499f-8bfb-43328f560410", "openfda": {"unii": ["229809935B"], "rxcui": ["991147"], "spl_set_id": ["d5bd3e97-b3f6-4bc2-9fb7-02921be35cdb"], "manufacturer_name": ["VistaPharm, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE (66689-694-79)", "package_ndc": "66689-694-79", "marketing_start_date": "20091030"}, {"sample": false, "description": "4000 mL in 1 BOTTLE (66689-694-88)", "package_ndc": "66689-694-88", "marketing_start_date": "20240819"}], "brand_name": "Methadone Hydrochloride", "product_id": "66689-694_a139d04a-25e0-499f-8bfb-43328f560410", "dosage_form": "CONCENTRATE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "66689-694", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "VistaPharm, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA040088", "marketing_category": "ANDA", "marketing_start_date": "20091030", "listing_expiration_date": "20271231"}