Calcitriol - 23155-119-01 - (Calcitriol)

Alphabetical Index


Drug Information of Calcitriol

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)

Labeler Information of Calcitriol

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 Information of Calcitriol

Package NDC: 23155-119-01
Package Description: 100 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (23155-119-01)

NDC Information of Calcitriol

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]

Complete Information of Calcitriol


General Information