Package 0904-7417-61

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7417-61
Digits Only 0904741761
Product NDC 0904-7417
Product ID 0904-7417_51c895c4-90fb-4d88-9032-beea257bec6c
Description

100 BLISTER PACK in 1 CARTON (0904-7417-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-01-03
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": ["ORAL"], "spl_id": "51c895c4-90fb-4d88-9032-beea257bec6c", "openfda": {"unii": ["229809935B"], "rxcui": ["864706"], "spl_set_id": ["db52fdc0-765a-4fad-a8f9-ef98c6e4b898"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7417-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7417-61", "marketing_start_date": "20240103"}], "brand_name": "METHADONE HYDROCHLORIDE", "product_id": "0904-7417_51c895c4-90fb-4d88-9032-beea257bec6c", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0904-7417", "dea_schedule": "CII", "generic_name": "METHADONE HYDROCHLORIDE", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHADONE HYDROCHLORIDE", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA088109", "marketing_category": "ANDA", "marketing_start_date": "20240103", "listing_expiration_date": "20261231"}