Package 81298-7500-1

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 81298-7500-1
Digits Only 8129875001
Product NDC 81298-7500
Product ID 81298-7500_46a3297c-98d2-48ef-a7a9-9776ed80e0bd
Description

1 VIAL, GLASS in 1 CARTON (81298-7500-1) / 20 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2025-06-28
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": ["INTRAVENOUS"], "spl_id": "46a3297c-98d2-48ef-a7a9-9776ed80e0bd", "openfda": {"unii": ["229809935B"], "rxcui": ["864714"], "spl_set_id": ["f453f1b9-d46e-4be8-835d-dbeb9d98a149"], "manufacturer_name": ["Long Grove Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (81298-7500-1)  / 20 mL in 1 VIAL, GLASS", "package_ndc": "81298-7500-1", "marketing_start_date": "20250628"}], "brand_name": "Methadone Hydrochloride", "product_id": "81298-7500_46a3297c-98d2-48ef-a7a9-9776ed80e0bd", "dosage_form": "INJECTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "81298-7500", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "Long Grove Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "200 mg/20mL"}], "application_number": "ANDA208306", "marketing_category": "ANDA", "marketing_start_date": "20250628", "listing_expiration_date": "20261231"}