Felbamate (Taro Pharmaceuticals U.S.A., Inc.)
Welcome to the PulseAid listing for the Felbamate drug offered from Taro Pharmaceuticals U.S.A., Inc.. This Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [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: | Taro Pharmaceuticals U.S.A., Inc. |
NON-PROPRIETARY NAME: | Felbamate |
SUBSTANCE NAME: | FELBAMATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
ROUTE: | ORAL |
DOSAGE FORM: | SUSPENSION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2017-06-16 |
END MARKETING DATE: | 0000-00-00 |
Felbamate HUMAN PRESCRIPTION DRUG Details:
Item Description | Felbamate from Taro Pharmaceuticals U.S.A., Inc. |
LABELER NAME: | Taro Pharmaceuticals U.S.A., Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 600(mg/5mL) |
START MARKETING DATE: | 2017-06-16 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 51672-4172_ff558824-b008-4b94-8aa5-d7818bc27a4f |
PRODUCT NDC: | 51672-4172 |
APPLICATION NUMBER: | ANDA206314 |
Other FELBAMATE Pharmaceutical Manufacturers / Labelers: