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Calcipotriene - 0781-7117-83 - (Calcipotriene)

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Drug Information of Calcipotriene

Product NDC: 0781-7117
Proprietary Name: Calcipotriene
Non Proprietary Name: Calcipotriene
Active Ingredient(s): .05    mg/g & nbsp;   Calcipotriene
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Calcipotriene

Product NDC: 0781-7117
Labeler Name: Sandoz Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200935
Marketing Category: ANDA
Start Marketing Date: 20120727

Package Information of Calcipotriene

Package NDC: 0781-7117-83
Package Description: 1 TUBE in 1 CARTON (0781-7117-83) > 120 g in 1 TUBE

NDC Information of Calcipotriene

NDC Code 0781-7117-83
Proprietary Name Calcipotriene
Package Description 1 TUBE in 1 CARTON (0781-7117-83) > 120 g in 1 TUBE
Product NDC 0781-7117
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Calcipotriene
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120727
Marketing Category Name ANDA
Labeler Name Sandoz Inc.
Substance Name CALCIPOTRIENE
Strength Number .05
Strength Unit mg/g
Pharmaceutical Classes Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC]

Complete Information of Calcipotriene


General Information