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"63032-031-50" National Drug Code (NDC)

Olux 50 g in 1 CAN (63032-031-50)
(Stiefel Laboratories Inc)

NDC Code63032-031-50
Package Description50 g in 1 CAN (63032-031-50)
Product NDC63032-031
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOlux
Non-Proprietary NameClobetasol Propionate
Dosage FormAEROSOL, FOAM
UsageTOPICAL
Start Marketing Date20001115
End Marketing Date20141231
Marketing Category NameNDA
Application NumberNDA021142
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/63032-031-50





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