| NDC Code | 47335-410-83 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (47335-410-83) |
|---|
| Product NDC | 47335-410 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Sumatriptan And Naproxen Sodium |
|---|
| Non-Proprietary Name | Sumatriptan And Naproxen Sodium |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20180720 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202803 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | NAPROXEN SODIUM; SUMATRIPTAN SUCCINATE |
|---|
| Strength | 500; 85 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], Serotonin 1b Receptor Agonists [MoA], Serotonin 1d Receptor Agonists [MoA], Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
|---|