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Calcipotriene
Calcipotriene - 0781-7117-35 - (Calcipotriene)
Drug Information of Calcipotriene
| Product NDC: | 0781-7117 |
| Proprietary Name: | Calcipotriene |
| Non Proprietary Name: | Calcipotriene |
| Active Ingredient(s): | .05 mg/g & nbsp; Calcipotriene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Calcipotriene
| Product NDC: | 0781-7117 |
| Labeler Name: | Sandoz Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200935 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120727 |
Package Information of Calcipotriene
| Package NDC: | 0781-7117-35 |
| Package Description: | 1 TUBE in 1 CARTON (0781-7117-35) > 60 g in 1 TUBE |
NDC Information of Calcipotriene
| NDC Code | 0781-7117-35 |
| Proprietary Name | Calcipotriene |
| Package Description | 1 TUBE in 1 CARTON (0781-7117-35) > 60 g in 1 TUBE |
| Product NDC | 0781-7117 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Calcipotriene |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120727 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc. |
| Substance Name | CALCIPOTRIENE |
| Strength Number | .05 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC] |
