Hydroxychloroquine Sulfate (Sandoz Inc)
Welcome to the PulseAid listing for the Hydroxychloroquine Sulfate drug offered from Sandoz 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: | Sandoz 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: | 1995-11-30 |
END MARKETING DATE: | 0000-00-00 |
Hydroxychloroquine Sulfate HUMAN PRESCRIPTION DRUG Details:
Item Description | Hydroxychloroquine Sulfate from Sandoz Inc |
LABELER NAME: | Sandoz Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 200(mg/1) |
START MARKETING DATE: | 1995-11-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0781-1407_9f44bec8-a0de-42a5-b207-355f274afd08 |
PRODUCT NDC: | 0781-1407 |
APPLICATION NUMBER: | ANDA040104 |
Other HYDROXYCHLOROQUINE SULFATE Pharmaceutical Manufacturers / Labelers: