| NDC Code | 43063-870-02 |
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| Package Description | 2 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-870-02) |
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| Product NDC | 43063-870 |
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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 | 20100412 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090469 |
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| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
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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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