desoximetasone
Desoximetasone Cream USP, 0.25%
Approved
Approval ID
b780701b-5572-48bc-a5f4-00248eaddd3b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 5, 2022
Manufacturers
FDA
Zydus Lifesciences Limited
DUNS: 918596198
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
desoximetasone
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code70771-1437
Application NumberANDA205620
Product Classification
M
Marketing Category
C73584
G
Generic Name
desoximetasone
Product Specifications
Route of AdministrationTOPICAL
Effective DateNovember 5, 2022
FDA Product Classification
INGREDIENTS (8)
DESOXIMETASONEActive
Quantity: 2.5 mg in 1 g
Code: 4E07GXB7AU
Classification: ACTIB
CETOSTEARYL ALCOHOLInactive
Code: 2DMT128M1S
Classification: IACT
ISOPROPYL MYRISTATEInactive
Code: 0RE8K4LNJS
Classification: IACT
EDETATE DISODIUMInactive
Code: 7FLD91C86K
Classification: IACT
LANOLIN ALCOHOLSInactive
Code: 884C3FA9HE
Classification: IACT
MINERAL OILInactive
Code: T5L8T28FGP
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
PETROLATUMInactive
Code: 4T6H12BN9U
Classification: IACT