Package 0406-2540-01

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0406-2540-01
Digits Only 0406254001
Product NDC 0406-2540
Product ID 0406-2540_991d6748-896f-42c1-88d6-fe1e77275181
Description

100 TABLET in 1 BOTTLE (0406-2540-01)

Marketing

Marketing Status
Marketed Since 2005-07-12
Brand methadone hydrochloride
Generic methadone hydrochloride
Sample Package No

Linked Drug Pages (1)

METHADOSE DISPERSIBLE, METHADONE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "991d6748-896f-42c1-88d6-fe1e77275181", "openfda": {"upc": ["0304060540347", "0304062540017"], "unii": ["229809935B"], "rxcui": ["864978", "864980"], "spl_set_id": ["544483e6-6f9d-4371-9e93-313e54e0ea05"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0406-2540-01)", "package_ndc": "0406-2540-01", "marketing_start_date": "20050712"}], "brand_name": "METHADONE HYDROCHLORIDE", "product_id": "0406-2540_991d6748-896f-42c1-88d6-fe1e77275181", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0406-2540", "dea_schedule": "CII", "generic_name": "METHADONE HYDROCHLORIDE", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHADONE HYDROCHLORIDE", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA077142", "marketing_category": "ANDA", "marketing_start_date": "20050712", "listing_expiration_date": "20261231"}