Moxifloxacin Hydrochloride (Teva Pharmaceuticals USA, Inc.)
Welcome to the PulseAid listing for the Moxifloxacin Hydrochloride drug offered from Teva Pharmaceuticals USA, 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: | Teva Pharmaceuticals USA, 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, FILM COATED |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2014-02-19 |
| END MARKETING DATE: | 0000-00-00 |
Moxifloxacin Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Moxifloxacin Hydrochloride from Teva Pharmaceuticals USA, Inc. |
| LABELER NAME: | Teva Pharmaceuticals USA, Inc. |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 400(mg/1) |
| START MARKETING DATE: | 2014-02-19 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0093-7387_d1ad23f3-e255-4575-b011-a7c65b48534e |
| PRODUCT NDC: | 0093-7387 |
| APPLICATION NUMBER: | ANDA077437 |
Other MOXIFLOXACIN HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
