Moxifloxacin (Lupin Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the Moxifloxacin drug offered from Lupin Pharmaceuticals, 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: | Lupin Pharmaceuticals, Inc. |
| NON-PROPRIETARY NAME: | Moxifloxacin |
| SUBSTANCE NAME: | MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
| ROUTE: | OPHTHALMIC |
| DOSAGE FORM: | SOLUTION/ DROPS |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2017-07-01 |
| END MARKETING DATE: | 0000-00-00 |
Moxifloxacin HUMAN PRESCRIPTION DRUG Details:
| Item Description | Moxifloxacin from Lupin Pharmaceuticals, Inc. |
| LABELER NAME: | Lupin Pharmaceuticals, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 5(mg/mL) |
| START MARKETING DATE: | 2017-07-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 68180-422_cf9069f5-b5be-49a7-bcd0-5f3e26aef7f9 |
| PRODUCT NDC: | 68180-422 |
| APPLICATION NUMBER: | ANDA202867 |
Other MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE Pharmaceutical Manufacturers / Labelers:
