Package 50090-7577-0
Brand: metformin hydrochloride
Generic: metformin hydrochloridePackage Facts
Identity
Package NDC
50090-7577-0
Digits Only
5009075770
Product NDC
50090-7577
Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7577-0)
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": "acd062d5-25ff-4e49-8605-30cbee1d0258", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["2d68fd88-c591-4577-a7c3-901338bdaf90"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7577-0)", "package_ndc": "50090-7577-0", "marketing_start_date": "20250609"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "50090-7577_acd062d5-25ff-4e49-8605-30cbee1d0258", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-7577", "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": "ANDA217631", "marketing_category": "ANDA", "marketing_start_date": "20231006", "listing_expiration_date": "20261231"}