Hydroxychloroquine sulfate (Zydus Pharmaceuticals (USA) Inc.)
Welcome to the PulseAid listing for the Hydroxychloroquine sulfate drug offered from Zydus Pharmaceuticals (USA) Inc.. 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: | Zydus Pharmaceuticals (USA) Inc. |
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: | ANDA |
START MARKETING DATE: | 2008-01-03 |
END MARKETING DATE: | 0000-00-00 |
Hydroxychloroquine sulfate HUMAN PRESCRIPTION DRUG Details:
Item Description | Hydroxychloroquine sulfate from Zydus Pharmaceuticals (USA) Inc. |
LABELER NAME: | Zydus Pharmaceuticals (USA) Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 200(mg/1) |
START MARKETING DATE: | 2008-01-03 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 68382-096_1af646d4-dcd5-4357-a150-402a985c4bd3 |
PRODUCT NDC: | 68382-096 |
APPLICATION NUMBER: | ANDA040657 |
Other HYDROXYCHLOROQUINE SULFATE Pharmaceutical Manufacturers / Labelers: