Chloramphenicol Sodium Succinate (Fresenius Kabi USA, LLC)
Welcome to the PulseAid listing for the Chloramphenicol Sodium Succinate drug offered from Fresenius Kabi USA, LLC. This Amphenicol-class Antibacterial [EPC],Amphenicols [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: | CHLORAMPHENICOL SODIUM SUCCINATE |
SUBSTANCE NAME: | CHLORAMPHENICOL SODIUM SUCCINATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Amphenicol-class Antibacterial [EPC],Amphenicols [Chemical/Ingredient] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2001-01-12 |
END MARKETING DATE: | 0000-00-00 |
Chloramphenicol Sodium Succinate HUMAN PRESCRIPTION DRUG Details:
Item Description | Chloramphenicol Sodium Succinate from Fresenius Kabi USA, LLC |
LABELER NAME: | Fresenius Kabi USA, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 1(g/10mL) |
START MARKETING DATE: | 2001-01-12 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 63323-011_00bd45d9-faa9-442c-a66b-3d18c004cfcc |
PRODUCT NDC: | 63323-011 |
APPLICATION NUMBER: | ANDA062365 |
Other CHLORAMPHENICOL SODIUM SUCCINATE Pharmaceutical Manufacturers / Labelers: