Package 63629-8501-1

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-8501-1
Digits Only 6362985011
Product NDC 63629-8501
Description

500 TABLET in 1 BOTTLE (63629-8501-1)

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": "57029a4d-1846-4811-8cd2-e6017905e8d6", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["a59327bd-a3ba-417b-9e91-4cd3a941e640"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (63629-8501-1)", "package_ndc": "63629-8501-1", "marketing_start_date": "20210518"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "63629-8501_57029a4d-1846-4811-8cd2-e6017905e8d6", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "63629-8501", "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"}