Ciprofloxacin (Watson Pharma, Inc.)
Welcome to the PulseAid listing for the Ciprofloxacin drug offered from Watson Pharma, Inc.. This Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient],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: | Watson Pharma, Inc. |
NON-PROPRIETARY NAME: | Ciprofloxacin |
SUBSTANCE NAME: | CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient],Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED, EXTENDED RELEASE |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2010-11-30 |
END MARKETING DATE: | 0000-00-00 |
Ciprofloxacin HUMAN PRESCRIPTION DRUG Details:
Item Description | Ciprofloxacin from Watson Pharma, Inc. |
LABELER NAME: | Watson Pharma, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 425.2; 574.9(mg/1; mg/1) |
START MARKETING DATE: | 2010-11-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 62037-938_b61a9cbe-8ae4-4f0f-9fbe-4bd1fe634043 |
PRODUCT NDC: | 62037-938 |
APPLICATION NUMBER: | ANDA077809 |
Other CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: