Product NDC: | 63304-241 |
Proprietary Name: | CALCITRIOL |
Non Proprietary Name: | CALCITRIOL |
Active Ingredient(s): | 1 ug/mL & nbsp; CALCITRIOL |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63304-241 |
Labeler Name: | Ranbaxy Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021068 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20090826 |
Package NDC: | 63304-241-59 |
Package Description: | 15 mL in 1 BOTTLE (63304-241-59) |
NDC Code | 63304-241-59 |
Proprietary Name | CALCITRIOL |
Package Description | 15 mL in 1 BOTTLE (63304-241-59) |
Product NDC | 63304-241 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CALCITRIOL |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20090826 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Ranbaxy Pharmaceuticals Inc. |
Substance Name | CALCITRIOL |
Strength Number | 1 |
Strength Unit | ug/mL |
Pharmaceutical Classes | Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC] |