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
NDC Product Code70752-153
Application NumberANDA211240
Marketing CategoryC73584
Route of AdministrationTOPICAL
Effective DateJanuary 10, 2024
Generic Nameclobetasol propionate
INGREDIENTS (1)
CLOBETASOL PROPIONATEActive
Quantity: 0.5 mg in 1 mL
Code: 779619577M
Classification: ACTIB