ISOSORBIDE MONONITRATE (Zydus Pharmaceuticals (USA) Inc.)
Welcome to the PulseAid listing for the ISOSORBIDE MONONITRATE drug offered from Zydus Pharmaceuticals (USA) Inc.. This Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE] 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: | Zydus Pharmaceuticals (USA) Inc. |
NON-PROPRIETARY NAME: | isosorbide mononitrate |
SUBSTANCE NAME: | ISOSORBIDE MONONITRATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2013-12-19 |
END MARKETING DATE: | 0000-00-00 |
ISOSORBIDE MONONITRATE HUMAN PRESCRIPTION DRUG Details:
Item Description | ISOSORBIDE MONONITRATE from Zydus Pharmaceuticals (USA) Inc. |
LABELER NAME: | Zydus Pharmaceuticals (USA) Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 30(mg/1) |
START MARKETING DATE: | 2013-12-19 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 68382-650_38b3edc6-8b4d-4855-8527-2229aadee33c |
PRODUCT NDC: | 68382-650 |
APPLICATION NUMBER: | ANDA075395 |
Other ISOSORBIDE MONONITRATE Pharmaceutical Manufacturers / Labelers: