| NDC Code | 68151-1668-8 |
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| Package Description | 1 mL in 1 CUP (68151-1668-8) |
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| Product NDC | 68151-1668 |
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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 | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20061226 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076960 |
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| Manufacturer | Carilion Materials Management |
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| Substance Name | ONDANSETRON HYDROCHLORIDE |
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| Strength | 4 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
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