| NDC Code | 35356-679-10 |
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| Package Description | 10 TABLET, FILM COATED in 1 BOTTLE (35356-679-10) |
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| Product NDC | 35356-679 |
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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 | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20070625 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077050 |
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| Manufacturer | Lake Erie Medical DBA Quality Care Products LLC |
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| Substance Name | ONDANSETRON HYDROCHLORIDE |
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| Strength | 8 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
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