Product NDC: | 63304-239 |
Proprietary Name: | CALCITRIOL |
Non Proprietary Name: | CALCITRIOL |
Active Ingredient(s): | .25 ug/1 & nbsp; CALCITRIOL |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63304-239 |
Labeler Name: | Ranbaxy Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018044 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20090826 |
Package NDC: | 63304-239-01 |
Package Description: | 100 CAPSULE in 1 BOTTLE (63304-239-01) |
NDC Code | 63304-239-01 |
Proprietary Name | CALCITRIOL |
Package Description | 100 CAPSULE in 1 BOTTLE (63304-239-01) |
Product NDC | 63304-239 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CALCITRIOL |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20090826 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Ranbaxy Pharmaceuticals Inc. |
Substance Name | CALCITRIOL |
Strength Number | .25 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC] |