Tobramycin (Fresenius Kabi USA, LLC)
Welcome to the PulseAid listing for the Tobramycin drug offered from Fresenius Kabi USA, LLC. This Aminoglycoside Antibacterial [EPC],Aminoglycosides [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: | TOBRAMYCIN SULFATE |
SUBSTANCE NAME: | TOBRAMYCIN SULFATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, POWDER, FOR SOLUTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2005-11-23 |
END MARKETING DATE: | 0000-00-00 |
Tobramycin HUMAN PRESCRIPTION DRUG Details:
Item Description | Tobramycin from Fresenius Kabi USA, LLC |
LABELER NAME: | Fresenius Kabi USA, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 1200(mg/30mL) |
START MARKETING DATE: | 2005-11-23 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 63323-303_07ee6545-c38a-4592-aa8d-0b1e605a345f |
PRODUCT NDC: | 63323-303 |
APPLICATION NUMBER: | NDA050789 |
Other TOBRAMYCIN SULFATE Pharmaceutical Manufacturers / Labelers: