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"63032-101-50" National Drug Code (NDC)

Olux-e 50 g in 1 CAN (63032-101-50)
(Stiefel Laboratories Inc)

NDC Code63032-101-50
Package Description50 g in 1 CAN (63032-101-50)
Product NDC63032-101
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOlux-e
Non-Proprietary NameClobetasol Propionate
Dosage FormAEROSOL, FOAM
UsageTOPICAL
Start Marketing Date20070212
End Marketing Date20150228
Marketing Category NameNDA
Application NumberNDA022013
ManufacturerStiefel Laboratories Inc
Substance NameCLOBETASOL PROPIONATE
Strength.5
Strength Unitmg/g
Pharmacy ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63032-101-50





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