Package 50090-7011-0

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7011-0
Digits Only 5009070110
Product NDC 50090-7011
Description

100 TABLET in 1 BOTTLE (50090-7011-0)

Marketing

Marketing Status
Marketed Since 2024-01-04
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": "19e4bfb8-2ed1-4a6b-adf5-853ad2953362", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["011de1a5-1ac0-4831-9e8d-26ec79ba2205"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-7011-0)", "package_ndc": "50090-7011-0", "marketing_start_date": "20240104"}], "brand_name": "Metformin Hydrochloride", "product_id": "50090-7011_19e4bfb8-2ed1-4a6b-adf5-853ad2953362", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-7011", "generic_name": "Metformin Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA090564", "marketing_category": "ANDA", "marketing_start_date": "20190626", "listing_expiration_date": "20261231"}