Calcitriol - 17478-932-01 - (Calcitriol)

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Drug Information of Calcitriol

Product NDC: 17478-932
Proprietary Name: Calcitriol
Non Proprietary Name: Calcitriol
Active Ingredient(s): 2    ug/mL & nbsp;   Calcitriol
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Calcitriol

Product NDC: 17478-932
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078066
Marketing Category: ANDA
Start Marketing Date: 20111014

Package Information of Calcitriol

Package NDC: 17478-932-01
Package Description: 10 AMPULE in 1 CARTON (17478-932-01) > 1 mL in 1 AMPULE

NDC Information of Calcitriol

NDC Code 17478-932-01
Proprietary Name Calcitriol
Package Description 10 AMPULE in 1 CARTON (17478-932-01) > 1 mL in 1 AMPULE
Product NDC 17478-932
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Calcitriol
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20111014
Marketing Category Name ANDA
Labeler Name Akorn, Inc.
Substance Name CALCITRIOL
Strength Number 2
Strength Unit ug/mL
Pharmaceutical Classes Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC]

Complete Information of Calcitriol


General Information