Dapsone - 49938-102-30 - (Dapsone)

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Drug Information of Dapsone

Product NDC: 49938-102
Proprietary Name: Dapsone
Non Proprietary Name: Dapsone
Active Ingredient(s): 25    mg/1 & nbsp;   Dapsone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Dapsone

Product NDC: 49938-102
Labeler Name: Jacobus Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086841
Marketing Category: ANDA
Start Marketing Date: 20080815

Package Information of Dapsone

Package NDC: 49938-102-30
Package Description: 2 BLISTER PACK in 1 CARTON (49938-102-30) > 15 TABLET in 1 BLISTER PACK

NDC Information of Dapsone

NDC Code 49938-102-30
Proprietary Name Dapsone
Package Description 2 BLISTER PACK in 1 CARTON (49938-102-30) > 15 TABLET in 1 BLISTER PACK
Product NDC 49938-102
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dapsone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080815
Marketing Category Name ANDA
Labeler Name Jacobus Pharmaceutical Company, Inc.
Substance Name DAPSONE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Sulfone [EPC],Sulfones [Chemical/Ingredient]

Complete Information of Dapsone


General Information