Thioridazine Hydrochloride (Sun Pharmaceutical Industries, Inc.)
Welcome to the PulseAid listing for the Thioridazine Hydrochloride drug offered from Sun Pharmaceutical Industries, Inc.. This Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] 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: | Sun Pharmaceutical Industries, Inc. |
| NON-PROPRIETARY NAME: | Thioridazine Hydrochloride |
| SUBSTANCE NAME: | THIORIDAZINE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, FILM COATED |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 1988-10-07 |
| END MARKETING DATE: | 0000-00-00 |
Thioridazine Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Thioridazine Hydrochloride from Sun Pharmaceutical Industries, Inc. |
| LABELER NAME: | Sun Pharmaceutical Industries, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10(mg/1) |
| START MARKETING DATE: | 1988-10-07 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 53489-148_2c96c6f9-3008-48ba-86ea-e9b83502da67 |
| PRODUCT NDC: | 53489-148 |
| APPLICATION NUMBER: | ANDA089953 |
Other THIORIDAZINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
