| Product NDC: | 23155-119 |
| Proprietary Name: | Calcitriol |
| Non Proprietary Name: | Calcitriol |
| Active Ingredient(s): | .5 ug/1 & nbsp; Calcitriol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 23155-119 |
| Labeler Name: | Heritage Pharmaceuticals Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091174 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130529 |
| Package NDC: | 23155-119-03 |
| Package Description: | 30 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (23155-119-03) |
| NDC Code | 23155-119-03 |
| Proprietary Name | Calcitriol |
| Package Description | 30 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (23155-119-03) |
| Product NDC | 23155-119 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Calcitriol |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20130529 |
| Marketing Category Name | ANDA |
| Labeler Name | Heritage Pharmaceuticals Inc |
| Substance Name | CALCITRIOL |
| Strength Number | .5 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC] |