Dovonex - 50222-260-99 - (Calcipotriene)

Alphabetical Index


Drug Information of Dovonex

Product NDC: 50222-260
Proprietary Name: Dovonex
Non Proprietary Name: Calcipotriene
Active Ingredient(s): 50    ug/g & nbsp;   Calcipotriene
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Dovonex

Product NDC: 50222-260
Labeler Name: LEO Pharma Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020554
Marketing Category: NDA
Start Marketing Date: 19961001

Package Information of Dovonex

Package NDC: 50222-260-99
Package Description: 25 CARTON in 1 CASE (50222-260-99) > 10 TUBE in 1 CARTON > 3 g in 1 TUBE

NDC Information of Dovonex

NDC Code 50222-260-99
Proprietary Name Dovonex
Package Description 25 CARTON in 1 CASE (50222-260-99) > 10 TUBE in 1 CARTON > 3 g in 1 TUBE
Product NDC 50222-260
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Calcipotriene
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19961001
Marketing Category Name NDA
Labeler Name LEO Pharma Inc.
Substance Name CALCIPOTRIENE
Strength Number 50
Strength Unit ug/g
Pharmaceutical Classes Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC]

Complete Information of Dovonex


General Information