Package 0527-1926-36

Brand: methadone hydrocloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0527-1926-36
Digits Only 0527192636
Product NDC 0527-1926
Description

1 BOTTLE, PLASTIC in 1 CARTON (0527-1926-36) / 30 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2021-03-03
Brand methadone hydrocloride
Generic methadone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6714ab49-287c-460f-84c6-4a2eb909b896", "openfda": {"upc": ["0305271926395"], "unii": ["229809935B"], "rxcui": ["991147"], "spl_set_id": ["119da5aa-bb8a-47cc-afb6-bcd2040a92a3"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (0527-1926-36)  / 30 mL in 1 BOTTLE, PLASTIC", "package_ndc": "0527-1926-36", "marketing_start_date": "20210303"}, {"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (0527-1926-39)", "package_ndc": "0527-1926-39", "marketing_start_date": "20210303"}], "brand_name": "Methadone Hydrocloride", "product_id": "0527-1926_6714ab49-287c-460f-84c6-4a2eb909b896", "dosage_form": "CONCENTRATE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0527-1926", "dea_schedule": "CII", "generic_name": "methadone hydrochloride", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrocloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA212094", "marketing_category": "ANDA", "marketing_start_date": "20210303", "listing_expiration_date": "20261231"}