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Ziprasidone
Ziprasidone - 52125-186-02 - (ZIPRASIDONE HYDROCHLORIDE)
Drug Information of Ziprasidone
| Product NDC: | 52125-186 |
| Proprietary Name: | Ziprasidone |
| Non Proprietary Name: | ZIPRASIDONE HYDROCHLORIDE |
| Active Ingredient(s): | 20 mg/1 & nbsp; ZIPRASIDONE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ziprasidone
| Product NDC: | 52125-186 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020825 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20130104 |
Package Information of Ziprasidone
| Package NDC: | 52125-186-02 |
| Package Description: | 30 CAPSULE in 1 BLISTER PACK (52125-186-02) |
NDC Information of Ziprasidone
| NDC Code | 52125-186-02 |
| Proprietary Name | Ziprasidone |
| Package Description | 30 CAPSULE in 1 BLISTER PACK (52125-186-02) |
| Product NDC | 52125-186 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ZIPRASIDONE HYDROCHLORIDE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130104 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | ZIPRASIDONE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC],Atypical Antipsychotic [EPC] |
