| NDC Code | 68462-158-11 |
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| Package Description | 10 TABLET, ORALLY DISINTEGRATING in 1 BOX, UNIT-DOSE (68462-158-11) |
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| Product NDC | 68462-158 |
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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 | TABLET, ORALLY DISINTEGRATING |
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| Usage | ORAL |
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| Start Marketing Date | 20070627 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078152 |
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| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
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| Substance Name | ONDANSETRON |
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| Strength | 8 |
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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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