Minoxidil
Minoxidil
Approved
Approval ID
934508f8-9252-4d48-ae91-0ce96454dc7b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 10, 2024
Manufacturers
FDA
Bryant Ranch Prepack
DUNS: 171714327
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Minoxidil
PRODUCT DETAILS
NDC Product Code63629-2231
Application NumberANDA071839
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateDecember 4, 2018
Generic NameMinoxidil
INGREDIENTS (6)
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
MINOXIDILActive
Quantity: 10 mg in 1 1
Code: 5965120SH1
Classification: ACTIB
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
ANHYDROUS LACTOSEInactive
Code: 3SY5LH9PMK
Classification: IACT
MICROCRYSTALLINE CELLULOSEInactive
Code: OP1R32D61U
Classification: IACT