| NDC Code | 36000-013-01 |
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| Package Description | 1 VIAL in 1 CARTON (36000-013-01) > 20 mL in 1 VIAL |
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| Product NDC | 36000-013 |
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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 | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20130313 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078288 |
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| Manufacturer | Baxter Healthcare Corporation |
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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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