Cefoxitin (Sagent Pharmaceuticals)
Welcome to the PulseAid listing for the Cefoxitin drug offered from Sagent Pharmaceuticals. 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: | Sagent Pharmaceuticals |
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: | INJECTION, POWDER, FOR SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2009-11-05 |
END MARKETING DATE: | 0000-00-00 |
Cefoxitin HUMAN PRESCRIPTION DRUG Details:
Item Description | Cefoxitin from Sagent Pharmaceuticals |
LABELER NAME: | Sagent Pharmaceuticals |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 1(g/1) |
START MARKETING DATE: | 2009-11-05 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 25021-109_afbba0c6-520f-48f4-a105-9b52af273714 |
PRODUCT NDC: | 25021-109 |
APPLICATION NUMBER: | ANDA065414 |
Other CEFOXITIN SODIUM Pharmaceutical Manufacturers / Labelers: