| NDC Code | 51662-1469-1 |
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| Package Description | 2 mL in 1 VIAL, SINGLE-DOSE (51662-1469-1) |
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| Product NDC | 51662-1469 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ondansetron |
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| Non-Proprietary Name | Ondansetron |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20191214 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077548 |
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| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
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| Substance Name | ONDANSETRON HYDROCHLORIDE |
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| Strength | 2 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC] |
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