ziprasidone hydrochloride (Sandoz Inc)
Welcome to the PulseAid listing for the ziprasidone hydrochloride drug offered from Sandoz Inc. This Atypical Antipsychotic [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Sandoz Inc |
| NON-PROPRIETARY NAME: | ziprasidone hydrochloride |
| SUBSTANCE NAME: | ZIPRASIDONE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Atypical Antipsychotic [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | CAPSULE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2013-02-13 |
| END MARKETING DATE: | 0000-00-00 |
ziprasidone hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | ziprasidone hydrochloride from Sandoz Inc |
| LABELER NAME: | Sandoz Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 20(mg/1) |
| START MARKETING DATE: | 2013-02-13 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0781-2164_3229e39f-4271-4075-981b-c68a56940e3a |
| PRODUCT NDC: | 0781-2164 |
| APPLICATION NUMBER: | ANDA077562 |
Other ZIPRASIDONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
