CLOBETASOL PROPIONATE
Clobetasol Propionate Topical Solution USP, 0.05% w/w Rx Only SCALP APPLICATION FOR TOPICAL DERMATOLOGIC USE ONLY NOT FOR OPHTHALMIC, ORAL, OR INTRAVAGINAL USE
Approved
Approval ID
5f6d2a57-92c9-4568-83d1-524de42182b4
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 10, 2024
Manufacturers
FDA
Quagen Pharmaceuticals LLC
DUNS: 073645339
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
clobetasol propionate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code70752-153
Application NumberANDA211240
Product Classification
M
Marketing Category
C73584
G
Generic Name
clobetasol propionate
Product Specifications
Route of AdministrationTOPICAL
Effective DateJanuary 10, 2024
FDA Product Classification
INGREDIENTS (1)
CLOBETASOL PROPIONATEActive
Quantity: 0.5 mg in 1 mL
Code: 779619577M
Classification: ACTIB