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TACLONEX SCALP - 0430-3240-96 - (calcipotriene 0.005% and betamethasone dipropionate 0.064%)

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Drug Information of TACLONEX SCALP

Product NDC: 0430-3240
Proprietary Name: TACLONEX SCALP
Non Proprietary Name: calcipotriene 0.005% and betamethasone dipropionate 0.064%
Active Ingredient(s): .643; 50    mg/g; ug/g & nbsp;   calcipotriene 0.005% and betamethasone dipropionate 0.064%
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY, METERED
Coding System: National Drug Codes(NDC)

Labeler Information of TACLONEX SCALP

Product NDC: 0430-3240
Labeler Name: Warner Chilcott (US), LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022185
Marketing Category: NDA
Start Marketing Date: 20080601

Package Information of TACLONEX SCALP

Package NDC: 0430-3240-96
Package Description: 40 CARTON in 1 CASE (0430-3240-96) > 1 BOTTLE in 1 CARTON > 4 g in 1 BOTTLE

NDC Information of TACLONEX SCALP

NDC Code 0430-3240-96
Proprietary Name TACLONEX SCALP
Package Description 40 CARTON in 1 CASE (0430-3240-96) > 1 BOTTLE in 1 CARTON > 4 g in 1 BOTTLE
Product NDC 0430-3240
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name calcipotriene 0.005% and betamethasone dipropionate 0.064%
Dosage Form Name SPRAY, METERED
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 SCALP


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