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OLUX
OLUX - 63032-031-00 - (clobetasol propionate)
Drug Information of OLUX
| Product NDC: | 63032-031 |
| Proprietary Name: | OLUX |
| Non Proprietary Name: | clobetasol propionate |
| Active Ingredient(s): | .5 mg/g & nbsp; clobetasol propionate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OLUX
| Product NDC: | 63032-031 |
| Labeler Name: | Stiefel Laboratories Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021142 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20001115 |
Package Information of OLUX
| Package NDC: | 63032-031-00 |
| Package Description: | 100 g in 1 CAN (63032-031-00) |
NDC Information of OLUX
| NDC Code | 63032-031-00 |
| Proprietary Name | OLUX |
| Package Description | 100 g in 1 CAN (63032-031-00) |
| Product NDC | 63032-031 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | clobetasol propionate |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20001115 |
| Marketing Category Name | NDA |
| Labeler Name | Stiefel Laboratories Inc |
| Substance Name | CLOBETASOL PROPIONATE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
