Hydroxychloroquine Sulfate (Northstar RxLLC)
Welcome to the PulseAid listing for the Hydroxychloroquine Sulfate drug offered from Northstar RxLLC. 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: | Northstar RxLLC |
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: | 2015-12-18 |
END MARKETING DATE: | 0000-00-00 |
Hydroxychloroquine Sulfate HUMAN PRESCRIPTION DRUG Details:
Item Description | Hydroxychloroquine Sulfate from Northstar RxLLC |
LABELER NAME: | Northstar RxLLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 200(mg/1) |
START MARKETING DATE: | 2015-12-18 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 16714-474_0fd6ecfd-3e5d-4553-8609-326ef96b27fb |
PRODUCT NDC: | 16714-474 |
APPLICATION NUMBER: | ANDA040104 |
Other HYDROXYCHLOROQUINE SULFATE Pharmaceutical Manufacturers / Labelers: