Package 63629-8503-1

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-8503-1
Digits Only 6362985031
Product NDC 63629-8503
Description

500 TABLET in 1 BOTTLE (63629-8503-1)

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": "df9541d1-769e-4b35-9da7-59fdad1632bf", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["a79d2674-071f-4641-9b11-406e02c5530a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (63629-8503-1)", "package_ndc": "63629-8503-1", "marketing_start_date": "20210518"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "63629-8503_df9541d1-769e-4b35-9da7-59fdad1632bf", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "63629-8503", "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": "1000 mg/1"}], "application_number": "ANDA203769", "marketing_category": "ANDA", "marketing_start_date": "20150201", "listing_expiration_date": "20261231"}