| NDC Code | 68071-4191-2 |
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| Package Description | 2 mL in 1 BOTTLE, GLASS (68071-4191-2) |
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| Product NDC | 68071-4191 |
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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 | INJECTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20120615 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079224 |
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| Manufacturer | NuCare Pharmaceuticals,Inc. |
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| Substance Name | ONDANSETRON HYDROCHLORIDE |
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| Strength | 2 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
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