Package 66689-820-10

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 66689-820-10
Digits Only 6668982010
Product NDC 66689-820
Product ID 66689-820_3cf3250f-2b57-4073-856f-3777bd6d7c1c
Description

100 TABLET in 1 BOTTLE (66689-820-10)

Marketing

Marketing Status
Discontinued 2027-02-28
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": ["ORAL"], "spl_id": "3cf3250f-2b57-4073-856f-3777bd6d7c1c", "openfda": {"unii": ["229809935B"], "rxcui": ["864706"], "spl_set_id": ["4c8b541c-33e8-4969-b258-af150808d46e"], "manufacturer_name": ["VistaPharm, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (66689-820-10)", "package_ndc": "66689-820-10", "marketing_end_date": "20270228", "marketing_start_date": "20181122"}], "brand_name": "Methadone Hydrochloride", "product_id": "66689-820_3cf3250f-2b57-4073-856f-3777bd6d7c1c", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "66689-820", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "VistaPharm, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA040241", "marketing_category": "ANDA", "marketing_end_date": "20270228", "marketing_start_date": "20181122"}