Oxcarbazepine (Sandoz Inc)
Welcome to the PulseAid listing for the Oxcarbazepine drug offered from Sandoz 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: | Sandoz Inc |
NON-PROPRIETARY NAME: | oxcarbazepine |
SUBSTANCE NAME: | OXCARBAZEPINE |
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: | NDA AUTHORIZED GENERIC |
START MARKETING DATE: | 2001-05-30 |
END MARKETING DATE: | 0000-00-00 |
Oxcarbazepine HUMAN PRESCRIPTION DRUG Details:
Item Description | Oxcarbazepine from Sandoz Inc |
LABELER NAME: | Sandoz Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 60(mg/mL) |
START MARKETING DATE: | 2001-05-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0781-6270_e3595f5a-dcea-4580-955c-e0dacef9d478 |
PRODUCT NDC: | 0781-6270 |
APPLICATION NUMBER: | NDA021285 |
Other OXCARBAZEPINE Pharmaceutical Manufacturers / Labelers: