Moxifloxacin Hydrochloride (Breckenridge Pharmaceutical, Inc.)
Welcome to the PulseAid listing for the Moxifloxacin Hydrochloride drug offered from Breckenridge Pharmaceutical, Inc.. 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: | Breckenridge Pharmaceutical, Inc. |
| NON-PROPRIETARY NAME: | Moxifloxacin Hydrochloride |
| SUBSTANCE NAME: | MOXIFLOXACIN HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2017-05-02 |
| END MARKETING DATE: | 0000-00-00 |
Moxifloxacin Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Moxifloxacin Hydrochloride from Breckenridge Pharmaceutical, Inc. |
| LABELER NAME: | Breckenridge Pharmaceutical, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 400(mg/1) |
| START MARKETING DATE: | 2017-05-02 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 51991-943_4e7c3467-c221-6034-e054-00144ff88e88 |
| PRODUCT NDC: | 51991-943 |
| APPLICATION NUMBER: | ANDA205348 |
Other MOXIFLOXACIN HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
