Home
>
National Drug Code (NDC)
>
Dapsone
Dapsone - 54868-3801-1 - (Dapsone)
Drug Information of Dapsone
| Product NDC: | 54868-3801 |
| Proprietary Name: | Dapsone |
| Non Proprietary Name: | Dapsone |
| Active Ingredient(s): | 100 mg/1 & nbsp; Dapsone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dapsone
| Product NDC: | 54868-3801 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA086842 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20051216 |
Package Information of Dapsone
| Package NDC: | 54868-3801-1 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (54868-3801-1) > 15 TABLET in 1 BLISTER PACK |
NDC Information of Dapsone
| NDC Code | 54868-3801-1 |
| Proprietary Name | Dapsone |
| Package Description | 2 BLISTER PACK in 1 CARTON (54868-3801-1) > 15 TABLET in 1 BLISTER PACK |
| Product NDC | 54868-3801 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dapsone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20051216 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | DAPSONE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Sulfone [EPC],Sulfones [Chemical/Ingredient] |
