| NDC Code | 43063-560-10 |
|---|
| Package Description | 10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-560-10) |
|---|
| Product NDC | 43063-560 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ondansetron |
|---|
| Non-Proprietary Name | Ondansetron |
|---|
| Dosage Form | TABLET, ORALLY DISINTEGRATING |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20070831 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078050 |
|---|
| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
|---|
| Substance Name | ONDANSETRON |
|---|
| Strength | 4 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
|---|