NDC Code | 70709-062-30 |
Package Description | 3 BLISTER PACK in 1 CARTON (70709-062-30) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
Product NDC | 70709-062 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Tascenso Odt |
Non-Proprietary Name | Fingolimod Lauryl Sulfate |
Dosage Form | TABLET, ORALLY DISINTEGRATING |
Usage | ORAL |
Start Marketing Date | 20230201 |
Marketing Category Name | NDA |
Application Number | NDA214962 |
Manufacturer | Cycle Pharmaceuticals Ltd |
Substance Name | FINGOLIMOD LAURYL SULFATE |
Strength | .25 |
Strength Unit | mg/1 |
Pharmacy Classes | Sphingosine 1-Phosphate Receptor Modulators [MoA], Sphingosine 1-phosphate Receptor Modulator [EPC] |