Package 63629-8502-1

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-8502-1
Digits Only 6362985021
Product NDC 63629-8502
Description

100 TABLET in 1 BOTTLE (63629-8502-1)

Marketing

Marketing Status
Marketed Since 2021-05-18
Brand metformin hydrochloride
Generic metformin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ee2f78b-9e0a-48e5-8306-814d9678c3d5", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["76879512-3ab4-4acf-92e6-bba0fb75dd0e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-8502-1)", "package_ndc": "63629-8502-1", "marketing_start_date": "20210518"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "63629-8502_4ee2f78b-9e0a-48e5-8306-814d9678c3d5", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "63629-8502", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA203769", "marketing_category": "ANDA", "marketing_start_date": "20150201", "listing_expiration_date": "20261231"}