Clemastine Fumarate (Northwind Pharmaceuticals, LLC)
Welcome to the PulseAid listing for the Clemastine Fumarate drug offered from Northwind Pharmaceuticals, LLC. This 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: | Northwind Pharmaceuticals, LLC |
NON-PROPRIETARY NAME: | Clemastine Fumarate |
SUBSTANCE NAME: | CLEMASTINE FUMARATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2014-04-28 |
END MARKETING DATE: | 0000-00-00 |
Clemastine Fumarate HUMAN PRESCRIPTION DRUG Details:
Item Description | Clemastine Fumarate from Northwind Pharmaceuticals, LLC |
LABELER NAME: | Northwind Pharmaceuticals, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 2.68(mg/1) |
START MARKETING DATE: | 2014-04-28 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 51655-425_82dfc095-30e3-441a-a9b6-5276a049f5a6 |
PRODUCT NDC: | 51655-425 |
APPLICATION NUMBER: | ANDA073283 |
Other CLEMASTINE FUMARATE Pharmaceutical Manufacturers / Labelers: