Latuda (Sunovion Pharmaceuticals Inc.)
Welcome to the PulseAid listing for the Latuda drug offered from Sunovion Pharmaceuticals 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: | Sunovion Pharmaceuticals Inc. |
| NON-PROPRIETARY NAME: | lurasidone hydrochloride |
| SUBSTANCE NAME: | LURASIDONE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Atypical Antipsychotic [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, FILM COATED |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2011-12-07 |
| END MARKETING DATE: | 0000-00-00 |
Latuda HUMAN PRESCRIPTION DRUG Details:
| Item Description | Latuda from Sunovion Pharmaceuticals Inc. |
| LABELER NAME: | Sunovion Pharmaceuticals Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 20(mg/1) |
| START MARKETING DATE: | 2011-12-07 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 63402-302_1ac4f198-aee2-4db4-917e-8896a31a36ec |
| PRODUCT NDC: | 63402-302 |
| APPLICATION NUMBER: | NDA200603 |
Other LURASIDONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
