Podofilox
Podofilox 0.5% Topical Solution Rx only
Approved
Approval ID
f502e134-63fd-4582-9290-c532a9d14948
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 21, 2010
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.
Podofilox
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54868-6198
Application NumberNDA019795
Product Classification
M
Marketing Category
C73605
G
Generic Name
Podofilox
Product Specifications
Route of AdministrationTOPICAL
Effective DateNovember 15, 2010
FDA Product Classification
INGREDIENTS (4)
PODOFILOXActive
Quantity: 5 mg in 1 mL
Code: L36H50F353
Classification: ACTIB
LACTIC ACIDInactive
Code: 33X04XA5AT
Classification: IACT
SODIUM LACTATEInactive
Code: TU7HW0W0QT
Classification: IACT
ALCOHOLInactive
Code: 3K9958V90M
Classification: IACT