| NDC Code | 80425-0469-1 |
|---|
| Package Description | 30 TABLET, ORALLY DISINTEGRATING in 1 BOX, UNIT-DOSE (80425-0469-1) |
|---|
| Product NDC | 80425-0469 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ondansetron |
|---|
| Non-Proprietary Name | Ondansetron |
|---|
| Dosage Form | TABLET, ORALLY DISINTEGRATING |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20241229 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078152 |
|---|
| Manufacturer | Advanced Rx of Tennessee, LLC |
|---|
| Substance Name | ONDANSETRON |
|---|
| Strength | 4 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC] |
|---|