| NDC Code | 70518-1585-1 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1585-1) |
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| Product NDC | 70518-1585 |
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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 | 20181024 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078539 |
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| Manufacturer | REMEDYREPACK INC. |
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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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