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:
