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SORILUX
SORILUX - 0145-2130-07 - (calcipotriene)
Drug Information of SORILUX
| Product NDC: | 0145-2130 |
| Proprietary Name: | SORILUX |
| Non Proprietary Name: | calcipotriene |
| Active Ingredient(s): | 50 ug/g & nbsp; calcipotriene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SORILUX
| Product NDC: | 0145-2130 |
| Labeler Name: | Stiefel Laboratories Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022563 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20101026 |
Package Information of SORILUX
| Package NDC: | 0145-2130-07 |
| Package Description: | 1 CAN in 1 CARTON (0145-2130-07) > 120 g in 1 CAN |
NDC Information of SORILUX
| NDC Code | 0145-2130-07 |
| Proprietary Name | SORILUX |
| Package Description | 1 CAN in 1 CARTON (0145-2130-07) > 120 g in 1 CAN |
| Product NDC | 0145-2130 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | calcipotriene |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20101026 |
| Marketing Category Name | NDA |
| Labeler Name | Stiefel Laboratories Inc |
| Substance Name | CALCIPOTRIENE |
| Strength Number | 50 |
| Strength Unit | ug/g |
| Pharmaceutical Classes | Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC] |
