| NDC Code | 63739-005-32 |
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| Package Description | 4 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-005-32) / 10 CAPSULE in 1 BLISTER PACK |
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| Product NDC | 63739-005 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ziprasidone Hydrochloride |
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| Non-Proprietary Name | Ziprasidone Hydrochloride |
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| Dosage Form | CAPSULE |
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| Usage | ORAL |
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| Start Marketing Date | 20120302 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077565 |
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| Manufacturer | McKesson Corporation dba SKY Packaging |
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| Substance Name | ZIPRASIDONE HYDROCHLORIDE |
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| Strength | 40 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Atypical Antipsychotic [EPC] |
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