Valproate Sodium (West-Ward Pharmaceuticals Corp)
Welcome to the PulseAid listing for the Valproate Sodium drug offered from West-Ward Pharmaceuticals Corp. This Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] 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: | West-Ward Pharmaceuticals Corp |
NON-PROPRIETARY NAME: | Valproate Sodium |
SUBSTANCE NAME: | VALPROATE SODIUM |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2010-02-17 |
END MARKETING DATE: | 0000-00-00 |
Valproate Sodium HUMAN PRESCRIPTION DRUG Details:
Item Description | Valproate Sodium from West-Ward Pharmaceuticals Corp |
LABELER NAME: | West-Ward Pharmaceuticals Corp |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 500(mg/5mL) |
START MARKETING DATE: | 2010-02-17 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0143-9785_149a8b03-e766-4409-9fd4-cdc45d34c73a |
PRODUCT NDC: | 0143-9785 |
APPLICATION NUMBER: | ANDA078523 |
Other VALPROATE SODIUM Pharmaceutical Manufacturers / Labelers: