Calcijex - 0074-8110-31 - (Calcitriol)

Alphabetical Index


Drug Information of Calcijex

Product NDC: 0074-8110
Proprietary Name: Calcijex
Non Proprietary Name: Calcitriol
Active Ingredient(s): 1    ug/mL & nbsp;   Calcitriol
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Calcijex

Product NDC: 0074-8110
Labeler Name: Abbott Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018874
Marketing Category: NDA
Start Marketing Date: 20100601

Package Information of Calcijex

Package NDC: 0074-8110-31
Package Description: 5 AMPULE in 1 CARTON (0074-8110-31) > 1 mL in 1 AMPULE

NDC Information of Calcijex

NDC Code 0074-8110-31
Proprietary Name Calcijex
Package Description 5 AMPULE in 1 CARTON (0074-8110-31) > 1 mL in 1 AMPULE
Product NDC 0074-8110
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Calcitriol
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20100601
Marketing Category Name NDA
Labeler Name Abbott Laboratories
Substance Name CALCITRIOL
Strength Number 1
Strength Unit ug/mL
Pharmaceutical Classes Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC]

Complete Information of Calcijex


General Information