Package 0641-6266-01

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0641-6266-01
Digits Only 0641626601
Product NDC 0641-6266
Product ID 0641-6266_821743df-67de-46a9-92c5-b530047a3192
Description

1 VIAL, MULTI-DOSE in 1 CARTON (0641-6266-01) / 20 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2025-06-12
Brand methadone hydrochloride
Generic methadone hydrochloride
Sample Package No

Linked Drug Pages (1)

Methadone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "821743df-67de-46a9-92c5-b530047a3192", "openfda": {"unii": ["229809935B"], "rxcui": ["864714"], "spl_set_id": ["1a6dbcb0-68f2-4f8b-94ee-baa2aa296293"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (0641-6266-01)  / 20 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0641-6266-01", "marketing_start_date": "20250612"}], "brand_name": "Methadone Hydrochloride", "product_id": "0641-6266_821743df-67de-46a9-92c5-b530047a3192", "dosage_form": "INJECTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0641-6266", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA218609", "marketing_category": "ANDA", "marketing_start_date": "20250612", "listing_expiration_date": "20261231"}