Package 72789-278-01
Brand: minoxidil
Generic: minoxidilPackage Facts
Identity
Package NDC
72789-278-01
Digits Only
7278927801
Product NDC
72789-278
Description
100 TABLET in 1 BOTTLE, PLASTIC (72789-278-01)
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": "2bedbd10-32ea-e55a-e063-6394a90a65f5", "openfda": {"nui": ["N0000175379", "N0000175564"], "upc": ["0372789278018"], "unii": ["5965120SH1"], "rxcui": ["197987"], "spl_set_id": ["5fea137a-bc88-4b24-85db-538c90ad1870"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-278-01)", "package_ndc": "72789-278-01", "marketing_start_date": "20221007"}], "brand_name": "MINOXIDIL", "product_id": "72789-278_2bedbd10-32ea-e55a-e063-6394a90a65f5", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "72789-278", "generic_name": "minoxidil", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MINOXIDIL", "active_ingredients": [{"name": "MINOXIDIL", "strength": "2.5 mg/1"}], "application_number": "ANDA072709", "marketing_category": "ANDA", "marketing_start_date": "19951214", "listing_expiration_date": "20261231"}