Package 50090-7535-0

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7535-0
Digits Only 5009075350
Product NDC 50090-7535
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7535-0)

Marketing

Marketing Status
Marketed Since 2025-04-08
Brand metformin hydrochloride
Generic metformin hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9d976647-7815-4c83-bf20-8484a30fa95e", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860981"], "spl_set_id": ["4f5389d2-dbcf-4fcb-9048-05953eb1fb05"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7535-0)", "package_ndc": "50090-7535-0", "marketing_start_date": "20250408"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "50090-7535_9d976647-7815-4c83-bf20-8484a30fa95e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-7535", "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": "750 mg/1"}], "application_number": "ANDA217631", "marketing_category": "ANDA", "marketing_start_date": "20231006", "listing_expiration_date": "20261231"}