Plaquenil (sanofi-aventis U.S. LLC)
Welcome to the PulseAid listing for the Plaquenil drug offered from sanofi-aventis U.S. LLC. This Antirheumatic Agent [EPC],Antimalarial [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: | sanofi-aventis U.S. LLC |
| NON-PROPRIETARY NAME: | Hydroxychloroquine Sulfate |
| SUBSTANCE NAME: | HYDROXYCHLOROQUINE SULFATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Antirheumatic Agent [EPC],Antimalarial [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, FILM COATED |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 1955-04-18 |
| END MARKETING DATE: | 0000-00-00 |
Plaquenil HUMAN PRESCRIPTION DRUG Details:
| Item Description | Plaquenil from sanofi-aventis U.S. LLC |
| LABELER NAME: | sanofi-aventis U.S. LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 200(mg/1) |
| START MARKETING DATE: | 1955-04-18 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0024-1562_c91c752e-ad6d-4b17-b1b5-2edc8a86856c |
| PRODUCT NDC: | 0024-1562 |
| APPLICATION NUMBER: | NDA009768 |
Other HYDROXYCHLOROQUINE SULFATE Pharmaceutical Manufacturers / Labelers:
