| Product NDC: | 43353-034 | 
| 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: | 43353-034 | 
| Labeler Name: | Aphena Pharma Solutions - Tennessee, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA076917 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20060327 | 
| Package NDC: | 43353-034-81 | 
| Package Description: | 800 CAPSULE in 1 BOTTLE, PLASTIC (43353-034-81) | 
| NDC Code | 43353-034-81 | 
| Proprietary Name | Calcitriol | 
| Package Description | 800 CAPSULE in 1 BOTTLE, PLASTIC (43353-034-81) | 
| Product NDC | 43353-034 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Calcitriol | 
| Dosage Form Name | CAPSULE | 
| Route Name | ORAL | 
| Start Marketing Date | 20060327 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Aphena Pharma Solutions - Tennessee, Inc. | 
| Substance Name | CALCITRIOL | 
| Strength Number | .25 | 
| Strength Unit | ug/1 | 
| Pharmaceutical Classes | Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC] |