| NDC Code | 62756-182-01 |
|---|
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (62756-182-01) > 20 mL in 1 VIAL, MULTI-DOSE |
|---|
| Product NDC | 62756-182 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ondansetron |
|---|
| Non-Proprietary Name | Ondansetron |
|---|
| Dosage Form | INJECTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20061226 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077172 |
|---|
| Manufacturer | Sun Pharmaceutical Industries Limited |
|---|
| Substance Name | ONDANSETRON HYDROCHLORIDE |
|---|
| Strength | 2 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
|---|