QUININE SULFATE (Lupin Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the QUININE SULFATE drug offered from Lupin Pharmaceuticals, Inc.. This 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: | Lupin Pharmaceuticals, Inc. |
NON-PROPRIETARY NAME: | QUININE SULFATE |
SUBSTANCE NAME: | QUININE SULFATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Antimalarial [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2015-08-04 |
END MARKETING DATE: | 0000-00-00 |
QUININE SULFATE HUMAN PRESCRIPTION DRUG Details:
Item Description | QUININE SULFATE from Lupin Pharmaceuticals, Inc. |
LABELER NAME: | Lupin Pharmaceuticals, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 324(mg/1) |
START MARKETING DATE: | 2015-08-04 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 68180-560_d7128c5d-b0de-4cdb-b17e-a6e91c558f30 |
PRODUCT NDC: | 68180-560 |
APPLICATION NUMBER: | ANDA203112 |
Other QUININE SULFATE Pharmaceutical Manufacturers / Labelers: