Calcitrene - 51672-5278-5 - (Calcipotriene)

Alphabetical Index


Drug Information of Calcitrene

Product NDC: 51672-5278
Proprietary Name: Calcitrene
Non Proprietary Name: Calcipotriene
Active Ingredient(s): .05    mg/g & nbsp;   Calcipotriene
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Calcitrene

Product NDC: 51672-5278
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090633
Marketing Category: ANDA
Start Marketing Date: 20100324

Package Information of Calcitrene

Package NDC: 51672-5278-5
Package Description: 10 TUBE in 1 CARTON (51672-5278-5) > 5 g in 1 TUBE

NDC Information of Calcitrene

NDC Code 51672-5278-5
Proprietary Name Calcitrene
Package Description 10 TUBE in 1 CARTON (51672-5278-5) > 5 g in 1 TUBE
Product NDC 51672-5278
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Calcipotriene
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20100324
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name CALCIPOTRIENE
Strength Number .05
Strength Unit mg/g
Pharmaceutical Classes Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC]

Complete Information of Calcitrene


General Information