Package 72865-120-01

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72865-120-01
Digits Only 7286512001
Product NDC 72865-120
Product ID 72865-120_639b24e8-927d-46ef-82f8-914a10528f21
Description

100 TABLET in 1 BOTTLE (72865-120-01)

Marketing

Marketing Status
Marketed Since 2019-01-03
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": "639b24e8-927d-46ef-82f8-914a10528f21", "openfda": {"upc": ["0372865121016", "0372865120019"], "unii": ["229809935B"], "rxcui": ["864706", "864718"], "spl_set_id": ["1a536622-dda3-41af-ab08-28e7c1bc9300"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72865-120-01)", "package_ndc": "72865-120-01", "marketing_start_date": "20190103"}], "brand_name": "Methadone Hydrochloride", "product_id": "72865-120_639b24e8-927d-46ef-82f8-914a10528f21", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72865-120", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "XLCare Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA211228", "marketing_category": "ANDA", "marketing_start_date": "20190103", "listing_expiration_date": "20261231"}