Product NDC: | 30698-143 |
Proprietary Name: | Rocaltrol |
Non Proprietary Name: | calcitriol |
Active Ingredient(s): | .25 ug/1 & nbsp; calcitriol |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, GELATIN COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 30698-143 |
Labeler Name: | Validus Pharmaceuticals LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018044 |
Marketing Category: | NDA |
Start Marketing Date: | 20090810 |
Package NDC: | 30698-143-23 |
Package Description: | 30 CAPSULE, GELATIN COATED in 1 BOTTLE (30698-143-23) |
NDC Code | 30698-143-23 |
Proprietary Name | Rocaltrol |
Package Description | 30 CAPSULE, GELATIN COATED in 1 BOTTLE (30698-143-23) |
Product NDC | 30698-143 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | calcitriol |
Dosage Form Name | CAPSULE, GELATIN COATED |
Route Name | ORAL |
Start Marketing Date | 20090810 |
Marketing Category Name | NDA |
Labeler Name | Validus Pharmaceuticals LLC |
Substance Name | CALCITRIOL |
Strength Number | .25 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC] |