Calcitriol - 0054-0007-25 - (Calcitriol)

Alphabetical Index


Drug Information of Calcitriol

Product NDC: 0054-0007
Proprietary Name: Calcitriol
Non Proprietary Name: Calcitriol
Active Ingredient(s): .25    ug/1 & nbsp;   Calcitriol
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Calcitriol

Product NDC: 0054-0007
Labeler Name: Roxane Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076917
Marketing Category: ANDA
Start Marketing Date: 20060327

Package Information of Calcitriol

Package NDC: 0054-0007-25
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (0054-0007-25)

NDC Information of Calcitriol

NDC Code 0054-0007-25
Proprietary Name Calcitriol
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (0054-0007-25)
Product NDC 0054-0007
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Calcitriol
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20060327
Marketing Category Name ANDA
Labeler Name Roxane Laboratories, Inc.
Substance Name CALCITRIOL
Strength Number .25
Strength Unit ug/1
Pharmaceutical Classes Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC]

Complete Information of Calcitriol


General Information