Package 63629-8503-1
Brand: metformin hydrochloride
Generic: metformin hydrochloridePackage 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
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"}