| NDC Code | 51672-4109-6 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (51672-4109-6) |
|---|
| Product NDC | 51672-4109 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ondansetron Hydrochloride |
|---|
| Non-Proprietary Name | Ondansetron Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20110328 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077729 |
|---|
| Manufacturer | Taro Pharmaceuticals U.S.A., Inc. |
|---|
| Substance Name | ONDANSETRON HYDROCHLORIDE |
|---|
| Strength | 8 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC] |
|---|