Quinine Sulfate (Teva Pharmaceuticals USA Inc)
Welcome to the PulseAid listing for the Quinine Sulfate drug offered from Teva Pharmaceuticals USA 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: | Teva Pharmaceuticals USA 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: | 2012-09-28 |
END MARKETING DATE: | 0000-00-00 |
Quinine Sulfate HUMAN PRESCRIPTION DRUG Details:
Item Description | Quinine Sulfate from Teva Pharmaceuticals USA Inc |
LABELER NAME: | Teva Pharmaceuticals USA Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 324(mg/1) |
START MARKETING DATE: | 2012-09-28 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0093-3002_1ba5baff-5f55-42ec-80d5-000181e12576 |
PRODUCT NDC: | 0093-3002 |
APPLICATION NUMBER: | ANDA091661 |
Other QUININE SULFATE Pharmaceutical Manufacturers / Labelers: