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: | 23155-119-01 |
Package Description: | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (23155-119-01) |
NDC Code | 23155-119-01 |
Proprietary Name | Calcitriol |
Package Description | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (23155-119-01) |
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] |