TACLONEX - 0430-3230-16 - (calcipotriene and betamethasone dipropionate)

Alphabetical Index


Drug Information of TACLONEX

Product NDC: 0430-3230
Proprietary Name: TACLONEX
Non Proprietary Name: calcipotriene and betamethasone dipropionate
Active Ingredient(s): .643; 50    mg/g; ug/g & nbsp;   calcipotriene and betamethasone dipropionate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of TACLONEX

Product NDC: 0430-3230
Labeler Name: Warner Chilcott (US), LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021852
Marketing Category: NDA
Start Marketing Date: 20080601

Package Information of TACLONEX

Package NDC: 0430-3230-16
Package Description: 50 CARTON in 1 CASE (0430-3230-16) > 1 TUBE in 1 CARTON > 100 g in 1 TUBE

NDC Information of TACLONEX

NDC Code 0430-3230-16
Proprietary Name TACLONEX
Package Description 50 CARTON in 1 CASE (0430-3230-16) > 1 TUBE in 1 CARTON > 100 g in 1 TUBE
Product NDC 0430-3230
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name calcipotriene and betamethasone dipropionate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20080601
Marketing Category Name NDA
Labeler Name Warner Chilcott (US), LLC
Substance Name BETAMETHASONE DIPROPIONATE; CALCIPOTRIENE
Strength Number .643; 50
Strength Unit mg/g; ug/g
Pharmaceutical Classes Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC]

Complete Information of TACLONEX


General Information