| NDC Code | 0078-0679-19 |
|---|
| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (0078-0679-19) > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0078-0679-61) |
|---|
| Product NDC | 0078-0679 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Zofran |
|---|
| Proprietary Name Suffix | Odt |
|---|
| Non-Proprietary Name | Ondansetron Hydrochloride |
|---|
| Dosage Form | TABLET, ORALLY DISINTEGRATING |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20170823 |
|---|
| End Marketing Date | 20191231 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA020781 |
|---|
| Manufacturer | Novartis Pharmaceuticals Corporation |
|---|
| Substance Name | ONDANSETRON |
|---|
| Strength | 4 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
|---|