| NDC Code | 64679-726-01 |
|---|
| Package Description | 5 VIAL, SINGLE-DOSE in 1 CARTON (64679-726-01) > 2 mL in 1 VIAL, SINGLE-DOSE (64679-726-03) |
|---|
| Product NDC | 64679-726 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ondansetron Hydrochloride |
|---|
| Non-Proprietary Name | Ondansetron Hydrochloride |
|---|
| Dosage Form | INJECTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20061227 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077716 |
|---|
| Manufacturer | Wockhardt USA LLC. |
|---|
| Substance Name | ONDANSETRON HYDROCHLORIDE |
|---|
| Strength | 2 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC] |
|---|