Clemastine Fumarate (Silarx Pharmaceuticals, Inc)
Welcome to the PulseAid listing for the Clemastine Fumarate drug offered from Silarx Pharmaceuticals, Inc. 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: | Silarx Pharmaceuticals, Inc |
NON-PROPRIETARY NAME: | Clemastine Fumarate |
SUBSTANCE NAME: | CLEMASTINE FUMARATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | SYRUP |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 1997-12-17 |
END MARKETING DATE: | 0000-00-00 |
Clemastine Fumarate HUMAN PRESCRIPTION DRUG Details:
Item Description | Clemastine Fumarate from Silarx Pharmaceuticals, Inc |
LABELER NAME: | Silarx Pharmaceuticals, Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 0.5(mg/mL) |
START MARKETING DATE: | 1997-12-17 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 54838-514_cf38b2c2-9171-49e8-9fd1-1f81967c0428 |
PRODUCT NDC: | 54838-514 |
APPLICATION NUMBER: | ANDA074884 |
Other CLEMASTINE FUMARATE Pharmaceutical Manufacturers / Labelers: