Package 63629-1027-1

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1027-1
Digits Only 6362910271
Product NDC 63629-1027
Product ID 63629-1027_c513c20b-ef58-4df1-8cce-ab397ef8e67c
Description

100 TABLET in 1 BOTTLE (63629-1027-1)

Marketing

Marketing Status
Marketed Since 2020-01-16
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": "c513c20b-ef58-4df1-8cce-ab397ef8e67c", "openfda": {"unii": ["229809935B"], "rxcui": ["864706"], "spl_set_id": ["3ce98ab4-346b-4680-b3e1-a8c29b3933af"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-1027-1)", "package_ndc": "63629-1027-1", "marketing_start_date": "20200116"}], "brand_name": "METHADONE HYDROCHLORIDE", "product_id": "63629-1027_c513c20b-ef58-4df1-8cce-ab397ef8e67c", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-1027", "dea_schedule": "CII", "generic_name": "METHADONE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHADONE HYDROCHLORIDE", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090635", "marketing_category": "ANDA", "marketing_start_date": "20120116", "listing_expiration_date": "20261231"}