| NDC Code | 0378-3702-59 |
|---|
| Package Description | 9 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (0378-3702-59) |
|---|
| Product NDC | 0378-3702 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Rizatriptan Benzoate |
|---|
| Non-Proprietary Name | Rizatriptan Benzoate |
|---|
| Dosage Form | TABLET, ORALLY DISINTEGRATING |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20121231 |
|---|
| End Marketing Date | 20200331 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078173 |
|---|
| Manufacturer | Mylan Pharmaceuticals Inc. |
|---|
| Substance Name | RIZATRIPTAN BENZOATE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
|---|