"10631-122-04" National Drug Code (NDC)

Ultravate 59 g in 1 BOTTLE (10631-122-04)
(Sun Pharmaceutical Industries, Inc.)

NDC Code10631-122-04
Package Description59 g in 1 BOTTLE (10631-122-04)
Product NDC10631-122
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameUltravate
Non-Proprietary NameHalobetasol Propionate
Dosage FormLOTION
UsageTOPICAL
Start Marketing Date20160301
Marketing Category NameNDA
Application NumberNDA208183
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameHALOBETASOL PROPIONATE
Strength.5
Strength Unitmg/g
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

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