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Calcipotriene
Calcipotriene - 0781-7092-61 - (Calcipotriene)
Drug Information of Calcipotriene
| Product NDC: | 0781-7092 |
| Proprietary Name: | Calcipotriene |
| Non Proprietary Name: | Calcipotriene |
| Active Ingredient(s): | .05 mg/mL & nbsp; Calcipotriene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Calcipotriene
| Product NDC: | 0781-7092 |
| Labeler Name: | Sandoz Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077029 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091120 |
Package Information of Calcipotriene
| Package NDC: | 0781-7092-61 |
| Package Description: | 60 mL in 1 BOTTLE, DROPPER (0781-7092-61) |
NDC Information of Calcipotriene
| NDC Code | 0781-7092-61 |
| Proprietary Name | Calcipotriene |
| Package Description | 60 mL in 1 BOTTLE, DROPPER (0781-7092-61) |
| Product NDC | 0781-7092 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Calcipotriene |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20091120 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc. |
| Substance Name | CALCIPOTRIENE |
| Strength Number | .05 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC] |
