| NDC Code | 51672-4138-6 |
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| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE (51672-4138-6) |
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| Product NDC | 51672-4138 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Granisetron Hydrochloride |
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| Non-Proprietary Name | Granisetron Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20100528 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090817 |
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| Manufacturer | Taro Pharmaceuticals U.S.A., Inc. |
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| Substance Name | GRANISETRON HYDROCHLORIDE |
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| Strength | 1 |
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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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