| Product NDC: | 66336-851 | 
| 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: | 66336-851 | 
| Labeler Name: | Dispensing Solutions, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | NDA018044 | 
| Marketing Category: | NDA AUTHORIZED GENERIC | 
| Start Marketing Date: | 20090826 | 
| Package NDC: | 66336-851-90 | 
| Package Description: | 90 CAPSULE in 1 BOTTLE (66336-851-90) | 
| NDC Code | 66336-851-90 | 
| Proprietary Name | CALCITRIOL | 
| Package Description | 90 CAPSULE in 1 BOTTLE (66336-851-90) | 
| Product NDC | 66336-851 | 
| 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 | Dispensing Solutions, Inc. | 
| Substance Name | CALCITRIOL | 
| Strength Number | .25 | 
| Strength Unit | ug/1 | 
| Pharmaceutical Classes | Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC] |