| NDC Code | 17856-0555-5 |
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| Package Description | 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0555-5) / 5 mL in 1 CUP, UNIT-DOSE |
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| Product NDC | 17856-0555 |
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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 Hydrochloride |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20110127 |
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| End Marketing Date | 20241130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091342 |
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| Manufacturer | ATLANTIC BIOLOGICALS CORP. |
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| Substance Name | ONDANSETRON HYDROCHLORIDE |
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| Strength | 4 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC] |
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