Package 51991-002-98

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51991-002-98
Digits Only 5199100298
Product NDC 51991-002
Product ID 51991-002_eec50ad6-d9ae-42df-ae5e-9cd75199148e
Description

1 VIAL, GLASS in 1 CARTON (51991-002-98) / 20 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2024-12-30
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": "eec50ad6-d9ae-42df-ae5e-9cd75199148e", "openfda": {"unii": ["229809935B"], "rxcui": ["864714"], "spl_set_id": ["13541167-95f4-4cb9-9d7d-3c1aced5c5f6"], "manufacturer_name": ["Breckenridge Pharmaceutical Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (51991-002-98)  / 20 mL in 1 VIAL, GLASS", "package_ndc": "51991-002-98", "marketing_start_date": "20241230"}], "brand_name": "Methadone Hydrochloride", "product_id": "51991-002_eec50ad6-d9ae-42df-ae5e-9cd75199148e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "51991-002", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "Breckenridge Pharmaceutical Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA218252", "marketing_category": "ANDA", "marketing_start_date": "20241230", "listing_expiration_date": "20261231"}