Package 50090-7578-0

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7578-0
Digits Only 5009075780
Product NDC 50090-7578
Description

90 TABLET, COATED in 1 BOTTLE (50090-7578-0)

Marketing

Marketing Status
Marketed Since 2025-06-16
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": "fcac2d10-44da-4beb-a588-3612698c4495", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["f6581ce6-0f9f-4887-ae83-4c6ecde619f3"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (50090-7578-0)", "package_ndc": "50090-7578-0", "marketing_start_date": "20250616"}], "brand_name": "Metformin Hydrochloride", "product_id": "50090-7578_fcac2d10-44da-4beb-a588-3612698c4495", "dosage_form": "TABLET, COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-7578", "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": "1000 mg/1"}], "application_number": "ANDA205096", "marketing_category": "ANDA", "marketing_start_date": "20240304", "listing_expiration_date": "20261231"}