| NDC Code | 36000-012-25 |
|---|
| Package Description | 25 VIAL in 1 CARTON (36000-012-25) / 2 mL in 1 VIAL |
|---|
| Product NDC | 36000-012 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ondansetron Hydrochloride |
|---|
| Non-Proprietary Name | Ondansetron Hydrochloride |
|---|
| Dosage Form | SOLUTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20130313 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078287 |
|---|
| 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] |
|---|