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Dapsone
Dapsone - 49938-102-30 - (Dapsone)
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] |
