Cefuroxime Sodium (Sagent Pharmaceuticals)
Welcome to the PulseAid listing for the Cefuroxime Sodium 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: | Cefuroxime Sodium |
| SUBSTANCE NAME: | CEFUROXIME 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: | 2016-09-01 |
| END MARKETING DATE: | 0000-00-00 |
Cefuroxime Sodium HUMAN PRESCRIPTION DRUG Details:
| Item Description | Cefuroxime Sodium from Sagent Pharmaceuticals |
| LABELER NAME: | Sagent Pharmaceuticals |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1.5(g/16mL) |
| START MARKETING DATE: | 2016-09-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 25021-119_480790e6-ea62-423e-964d-cfa4e8541c00 |
| PRODUCT NDC: | 25021-119 |
| APPLICATION NUMBER: | ANDA064125 |
Other CEFUROXIME SODIUM Pharmaceutical Manufacturers / Labelers: