Package 63629-9147-1

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-9147-1
Digits Only 6362991471
Product NDC 63629-9147
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-9147-1)

Marketing

Marketing Status
Marketed Since 2022-01-26
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": "f70200e9-9e16-40ee-a09f-04a418ae1d36", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860981"], "spl_set_id": ["93b0878d-b039-4479-8315-6dabf7e70611"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-9147-1)", "package_ndc": "63629-9147-1", "marketing_start_date": "20220126"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "63629-9147_f70200e9-9e16-40ee-a09f-04a418ae1d36", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "63629-9147", "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": "750 mg/1"}], "application_number": "ANDA076756", "marketing_category": "ANDA", "marketing_start_date": "20200806", "listing_expiration_date": "20261231"}