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Diflorasone Diacetate - 0168-0353-30 - (diflorasone diacetate)

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Drug Information of Diflorasone Diacetate

Product NDC: 0168-0353
Proprietary Name: Diflorasone Diacetate
Non Proprietary Name: diflorasone diacetate
Active Ingredient(s): .5    mg/g & nbsp;   diflorasone diacetate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Diflorasone Diacetate

Product NDC: 0168-0353
Labeler Name: E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076263
Marketing Category: ANDA
Start Marketing Date: 20021220

Package Information of Diflorasone Diacetate

Package NDC: 0168-0353-30
Package Description: 1 TUBE in 1 CARTON (0168-0353-30) > 30 g in 1 TUBE

NDC Information of Diflorasone Diacetate

NDC Code 0168-0353-30
Proprietary Name Diflorasone Diacetate
Package Description 1 TUBE in 1 CARTON (0168-0353-30) > 30 g in 1 TUBE
Product NDC 0168-0353
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diflorasone diacetate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20021220
Marketing Category Name ANDA
Labeler Name E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.
Substance Name DIFLORASONE DIACETATE
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Diflorasone Diacetate


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