Package 50090-7579-0

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7579-0
Digits Only 5009075790
Product NDC 50090-7579
Product ID 50090-7579_c7bc53cc-f250-45ff-a179-09c33ef470cd
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7579-0)

Marketing

Marketing Status
Marketed Since 2025-06-16
Brand metformin hydrochloride
Generic metformin hydrochloride
Sample Package No

Linked Drug Pages (1)

METFORMIN HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c7bc53cc-f250-45ff-a179-09c33ef470cd", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["784a6bbd-4f13-45ed-89c1-154b06721ed0"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7579-0)", "package_ndc": "50090-7579-0", "marketing_start_date": "20250616"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "50090-7579_c7bc53cc-f250-45ff-a179-09c33ef470cd", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-7579", "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": "ANDA201991", "marketing_category": "ANDA", "marketing_start_date": "20130301", "listing_expiration_date": "20261231"}