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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code10631-119
Application NumberNDA019968
Product Classification
M
Marketing Category
C73594
G
Generic Name
Halobetasol Propionate
Product Specifications
Effective DateNovember 8, 2012
FDA Product Classification