Cefoxitin (Fresenius Kabi USA, LLC)
Welcome to the PulseAid listing for the Cefoxitin drug offered from Fresenius Kabi USA, LLC. This Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] 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: | Fresenius Kabi USA, LLC |
NON-PROPRIETARY NAME: | Cefoxitin Sodium |
SUBSTANCE NAME: | CEFOXITIN SODIUM |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | POWDER, FOR SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2011-07-06 |
END MARKETING DATE: | 0000-00-00 |
Cefoxitin HUMAN PRESCRIPTION DRUG Details:
Item Description | Cefoxitin from Fresenius Kabi USA, LLC |
LABELER NAME: | Fresenius Kabi USA, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 1(g/1) |
START MARKETING DATE: | 2011-07-06 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 63323-341_2a9d1e7b-96ee-4e6c-a1e8-47b76b924422 |
PRODUCT NDC: | 63323-341 |
APPLICATION NUMBER: | ANDA065414 |
Other CEFOXITIN SODIUM Pharmaceutical Manufacturers / Labelers: