Moxifloxacin (Fresenius Kabi USA, LLC)
Welcome to the PulseAid listing for the Moxifloxacin drug offered from Fresenius Kabi USA, LLC. This Quinolone Antimicrobial [EPC],Quinolones [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: | MOXIFLOXACIN HYDROCHLORIDE |
| SUBSTANCE NAME: | MOXIFLOXACIN HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2015-03-18 |
| END MARKETING DATE: | 0000-00-00 |
Moxifloxacin HUMAN PRESCRIPTION DRUG Details:
| Item Description | Moxifloxacin from Fresenius Kabi USA, LLC |
| LABELER NAME: | Fresenius Kabi USA, LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 400(mg/250mL) |
| START MARKETING DATE: | 2015-03-18 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 63323-850_a23c58f0-408e-47d1-829f-5468c519ebd3 |
| PRODUCT NDC: | 63323-850 |
| APPLICATION NUMBER: | NDA205572 |
Other MOXIFLOXACIN HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
