Product NDC: | 45802-608 |
Proprietary Name: | calcitriol |
Non Proprietary Name: | calcitriol |
Active Ingredient(s): | 3 ug/g & nbsp; calcitriol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 45802-608 |
Labeler Name: | Perrigo New York Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022087 |
Marketing Category: | NDA |
Start Marketing Date: | 20120308 |
Package NDC: | 45802-608-01 |
Package Description: | 1 TUBE in 1 CARTON (45802-608-01) > 100 g in 1 TUBE |
NDC Code | 45802-608-01 |
Proprietary Name | calcitriol |
Package Description | 1 TUBE in 1 CARTON (45802-608-01) > 100 g in 1 TUBE |
Product NDC | 45802-608 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | calcitriol |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20120308 |
Marketing Category Name | NDA |
Labeler Name | Perrigo New York Inc |
Substance Name | CALCITRIOL |
Strength Number | 3 |
Strength Unit | ug/g |
Pharmaceutical Classes | Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC] |