| NDC Code | 0069-0700-12 |
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| Package Description | 6 BAG in 1 CASE (0069-0700-12) > 50 mL in 1 BAG |
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| Product NDC | 0069-0700 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ondansetron Hydrochloride And Dextrose |
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| Non-Proprietary Name | Ondansetron Hydrochloride And Dextrose |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20090501 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078308 |
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| Manufacturer | Pfizer Labs, Division of Pfizer Inc. |
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| Substance Name | ONDANSETRON HYDROCHLORIDE |
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| Strength | 32 |
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| Strength Unit | mg/50mL |
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| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
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