ELIQUIS (E.R. Squibb & Sons, L.L.C.)
Welcome to the PulseAid listing for the ELIQUIS drug offered from E.R. Squibb & Sons, L.L.C.. This Factor Xa Inhibitor [EPC],Factor Xa Inhibitors [MoA] 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: | E.R. Squibb & Sons, L.L.C. |
NON-PROPRIETARY NAME: | apixaban |
SUBSTANCE NAME: | APIXABAN |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Factor Xa Inhibitor [EPC],Factor Xa Inhibitors [MoA] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2012-12-28 |
END MARKETING DATE: | 0000-00-00 |
ELIQUIS HUMAN PRESCRIPTION DRUG Details:
Item Description | ELIQUIS from E.R. Squibb & Sons, L.L.C. |
LABELER NAME: | E.R. Squibb & Sons, L.L.C. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 2.5(mg/1) |
START MARKETING DATE: | 2012-12-28 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0003-0893_85dab2fd-ac9a-4279-92e2-c1c9cf83ffb2 |
PRODUCT NDC: | 0003-0893 |
APPLICATION NUMBER: | NDA202155 |
Other APIXABAN Pharmaceutical Manufacturers / Labelers: