Ultravate X
ULTRAVATE X(halobetasol propionate ointment) Ointment, 0.05%For Dermatological Use Only. Not for Ophthalmic Use.Rx only
Approved
Approval ID
21e4e0c0-18c7-480a-af4e-7b553fe8b68c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 8, 2012
Manufacturers
FDA
Ranbaxy Laboratories Inc.
DUNS: 169932519
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Halobetasol Propionate
PRODUCT DETAILS
NDC Product Code10631-119
Application NumberNDA019968
Marketing CategoryC73594
Route of AdministrationN/A
Effective DateNovember 8, 2012
Generic NameHalobetasol Propionate