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Calcipotriene
Calcipotriene - 0713-0318-53 - (Calcipotriene)
Drug Information of Calcipotriene
| Product NDC: | 0713-0318 |
| 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: | 0713-0318 |
| Labeler Name: | G & W Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078468 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110404 |
Package Information of Calcipotriene
| Package NDC: | 0713-0318-53 |
| Package Description: | 1 BOTTLE in 1 CARTON (0713-0318-53) > 60 mL in 1 BOTTLE |
NDC Information of Calcipotriene
| NDC Code | 0713-0318-53 |
| Proprietary Name | Calcipotriene |
| Package Description | 1 BOTTLE in 1 CARTON (0713-0318-53) > 60 mL in 1 BOTTLE |
| Product NDC | 0713-0318 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Calcipotriene |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110404 |
| Marketing Category Name | ANDA |
| Labeler Name | G & W Laboratories, Inc. |
| Substance Name | CALCIPOTRIENE |
| Strength Number | .05 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC] |
