| NDC Code | 82449-201-01 |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (82449-201-01) / 20 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 82449-201 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Proprietary Name | Ondansetron Hydrochloride |
| Non-Proprietary Name | Ondansetron Hydrochloride |
| Dosage Form | INJECTION |
| Usage | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20230930 |
| Marketing Category Name | ANDA |
| Application Number | ANDA078257 |
| Manufacturer | Steriscience Specialties Private Limited |
| Substance Name | ONDANSETRON HYDROCHLORIDE |
| Strength | 2 |
| Strength Unit | mg/mL |
| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC] |