ApexiCon E - 10337-395-08 - (diflorasone diacetate)

Alphabetical Index


Drug Information of ApexiCon E

Product NDC: 10337-395
Proprietary Name: ApexiCon E
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 ApexiCon E

Product NDC: 10337-395
Labeler Name: PharmaDerm 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 ApexiCon E

Package NDC: 10337-395-08
Package Description: 2 g in 1 TUBE (10337-395-08)

NDC Information of ApexiCon E

NDC Code 10337-395-08
Proprietary Name ApexiCon E
Package Description 2 g in 1 TUBE (10337-395-08)
Product NDC 10337-395
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 PharmaDerm 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 ApexiCon E


General Information