| NDC Code | 49349-858-08 |
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| Package Description | 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49349-858-08) |
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| Product NDC | 49349-858 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Zofran |
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| Non-Proprietary Name | Ondansetron Hydrochloride |
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| Dosage Form | TABLET, ORALLY DISINTEGRATING |
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| Usage | ORAL |
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| Start Marketing Date | 20111219 |
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| Marketing Category Name | NDA |
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| Application Number | NDA020781 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | ONDANSETRON HYDROCHLORIDE |
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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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