Package 67457-217-20

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67457-217-20
Digits Only 6745721720
Product NDC 67457-217
Product ID 67457-217_868dd5b8-2e28-475c-b6c3-bfc0a33fb793
Description

1 VIAL, MULTI-DOSE in 1 CARTON (67457-217-20) / 20 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2012-12-20
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": "868dd5b8-2e28-475c-b6c3-bfc0a33fb793", "openfda": {"unii": ["229809935B"], "rxcui": ["864714"], "spl_set_id": ["092d78eb-6423-495c-bf0d-e6532bea7138"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (67457-217-20)  / 20 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "67457-217-20", "marketing_start_date": "20121220"}], "brand_name": "Methadone Hydrochloride", "product_id": "67457-217_868dd5b8-2e28-475c-b6c3-bfc0a33fb793", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "67457-217", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "NDA021624", "marketing_category": "NDA", "marketing_start_date": "20121220", "listing_expiration_date": "20261231"}