Desoximetasone
Desoximetasone Cream USP, 0.05%, Cream USP, 0.25%Gel USP, 0.05%
Approved
Approval ID
caed3adf-fab7-43d4-a00b-b8bd9bfa06d1
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 8, 2009
Manufacturers
FDA
Physicians Total Care, Inc.
DUNS: 194123980
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 Code54868-2829
Application NumberANDA074904
Product Classification
M
Marketing Category
C73584
G
Generic Name
Desoximetasone
Product Specifications
Route of AdministrationTOPICAL
Effective DateJanuary 12, 2011
FDA Product Classification
INGREDIENTS (7)
WATERInactive
Code: 059QF0KO0R
Classification: IACT
DOCUSATE SODIUMInactive
Code: F05Q2T2JA0
Classification: IACT
ISOPROPYL MYRISTATEInactive
Code: 0RE8K4LNJS
Classification: IACT
EDETATE DISODIUMInactive
Code: 7FLD91C86K
Classification: IACT
TROLAMINEInactive
Code: 9O3K93S3TK
Classification: IACT
CARBOMER HOMOPOLYMER TYPE CInactive
Code: 4Q93RCW27E
Classification: IACT
DESOXIMETASONEActive
Quantity: 0.5 mg in 1 g
Code: 4E07GXB7AU
Classification: ACTIB