Package 50090-7587-0
Brand: metformin hydrochloride
Generic: metformin hydrochloridePackage Facts
Identity
Package NDC
50090-7587-0
Digits Only
5009075870
Product NDC
50090-7587
Description
90 TABLET in 1 BOTTLE (50090-7587-0)
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": "e5d066e4-47a6-4a2d-af78-e8d4e0cea3c8", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["51e1fe6e-a7fa-47a5-bbd5-73b275230c7f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7587-0)", "package_ndc": "50090-7587-0", "marketing_start_date": "20250630"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "50090-7587_e5d066e4-47a6-4a2d-af78-e8d4e0cea3c8", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-7587", "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": "ANDA203769", "marketing_category": "ANDA", "marketing_start_date": "20150201", "listing_expiration_date": "20261231"}