Dovonex - 50222-403-60 - (Calcipotriene)

Alphabetical Index


Drug Information of Dovonex

Product NDC: 50222-403
Proprietary Name: Dovonex
Non Proprietary Name: Calcipotriene
Active Ingredient(s): .05    mg/mL & nbsp;   Calcipotriene
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dovonex

Product NDC: 50222-403
Labeler Name: LEO Pharma Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020611
Marketing Category: NDA
Start Marketing Date: 19970601

Package Information of Dovonex

Package NDC: 50222-403-60
Package Description: 40 CARTON in 1 CASE (50222-403-60) > 1 BOTTLE in 1 CARTON > 60 mL in 1 BOTTLE

NDC Information of Dovonex

NDC Code 50222-403-60
Proprietary Name Dovonex
Package Description 40 CARTON in 1 CASE (50222-403-60) > 1 BOTTLE in 1 CARTON > 60 mL in 1 BOTTLE
Product NDC 50222-403
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Calcipotriene
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 19970601
Marketing Category Name NDA
Labeler Name LEO Pharma Inc.
Substance Name CALCIPOTRIENE
Strength Number .05
Strength Unit mg/mL
Pharmaceutical Classes Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC]

Complete Information of Dovonex


General Information