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Calcipotriene
Calcipotriene - 68462-310-65 - (Calcipotriene)
Drug Information of Calcipotriene
| Product NDC: | 68462-310 |
| Proprietary Name: | Calcipotriene |
| Non Proprietary Name: | Calcipotriene |
| Active Ingredient(s): | 50 ug/g & nbsp; Calcipotriene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Calcipotriene
| Product NDC: | 68462-310 |
| Labeler Name: | Glenmark Generics Inc., USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090633 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100324 |
Package Information of Calcipotriene
| Package NDC: | 68462-310-65 |
| Package Description: | 60 g in 1 TUBE (68462-310-65) |
NDC Information of Calcipotriene
| NDC Code | 68462-310-65 |
| Proprietary Name | Calcipotriene |
| Package Description | 60 g in 1 TUBE (68462-310-65) |
| Product NDC | 68462-310 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Calcipotriene |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20100324 |
| Marketing Category Name | ANDA |
| Labeler Name | Glenmark Generics Inc., USA |
| Substance Name | CALCIPOTRIENE |
| Strength Number | 50 |
| Strength Unit | ug/g |
| Pharmaceutical Classes | Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC] |
