| NDC Code | 10019-906-04 |
|---|
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (10019-906-04) > 20 mL in 1 VIAL, MULTI-DOSE (10019-906-05) |
|---|
| Product NDC | 10019-906 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ondansetron |
|---|
| Non-Proprietary Name | Ondansetron Hydrochloride |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20101119 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077365 |
|---|
| Manufacturer | Baxter Healthcare Corporation |
|---|
| Substance Name | ONDANSETRON HYDROCHLORIDE |
|---|
| Strength | 2 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
|---|