| NDC Code | 23155-378-41 |
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| Package Description | 10 VIAL in 1 CARTON (23155-378-41) > 2 mL in 1 VIAL (23155-378-31) |
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| Product NDC | 23155-378 |
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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 | INJECTION, SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20140219 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078945 |
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| Manufacturer | Heritage 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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