| NDC Code | 51991-735-32 |
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| Package Description | 1 BLISTER PACK in 1 CARTON (51991-735-32) / 2 TABLET in 1 BLISTER PACK |
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| Product NDC | 51991-735 |
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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 |
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| Usage | ORAL |
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| Start Marketing Date | 20090622 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078969 |
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| Manufacturer | Breckenridge Pharmaceutical, 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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