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Prednicarbate - 0168-0410-60 - (prednicarbate)

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Drug Information of Prednicarbate

Product NDC: 0168-0410
Proprietary Name: Prednicarbate
Non Proprietary Name: prednicarbate
Active Ingredient(s): 1    mg/g & nbsp;   prednicarbate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Prednicarbate

Product NDC: 0168-0410
Labeler Name: E. Fougera & Co., a division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077236
Marketing Category: ANDA
Start Marketing Date: 20070309

Package Information of Prednicarbate

Package NDC: 0168-0410-60
Package Description: 60 g in 1 TUBE (0168-0410-60)

NDC Information of Prednicarbate

NDC Code 0168-0410-60
Proprietary Name Prednicarbate
Package Description 60 g in 1 TUBE (0168-0410-60)
Product NDC 0168-0410
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name prednicarbate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20070309
Marketing Category Name ANDA
Labeler Name E. Fougera & Co., a division of Fougera Pharmaceuticals Inc.
Substance Name PREDNICARBATE
Strength Number 1
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Prednicarbate


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