Package 50090-7760-2
Brand: minoxidil
Generic: minoxidilPackage Facts
Identity
Package NDC
50090-7760-2
Digits Only
5009077602
Product NDC
50090-7760
Description
90 TABLET in 1 BOTTLE (50090-7760-2)
Marketing
Marketing Status
Brand
minoxidil
Generic
minoxidil
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9912a946-471e-4e0c-addf-373f401da0c9", "openfda": {"nui": ["N0000175379", "N0000175564"], "unii": ["5965120SH1"], "rxcui": ["197986"], "spl_set_id": ["f00f3370-0313-4ce0-be7d-80db4477d9ae"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7760-2)", "package_ndc": "50090-7760-2", "marketing_start_date": "20251106"}], "brand_name": "Minoxidil", "product_id": "50090-7760_9912a946-471e-4e0c-addf-373f401da0c9", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "50090-7760", "generic_name": "Minoxidil", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minoxidil", "active_ingredients": [{"name": "MINOXIDIL", "strength": "10 mg/1"}], "application_number": "ANDA071839", "marketing_category": "ANDA", "marketing_start_date": "19881114", "listing_expiration_date": "20261231"}