| NDC Code | 51655-415-53 |
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| Package Description | 10 TABLET, FILM COATED in 1 BOTTLE (51655-415-53) |
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| Product NDC | 51655-415 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ondansetron Hydrochloride |
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| Non-Proprietary Name | Ondansetron Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20171207 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078539 |
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| Manufacturer | Northwind Pharmaceuticals, LLC |
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| Substance Name | ONDANSETRON HYDROCHLORIDE |
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| Strength | 4 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC] |
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