Oxcarbazepine (Sun Pharmaceutical Industries Limited)
Welcome to the PulseAid listing for the Oxcarbazepine drug offered from Sun Pharmaceutical Industries Limited. 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: | Sun Pharmaceutical Industries Limited |
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: | TABLET, FILM COATED |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2007-10-09 |
END MARKETING DATE: | 0000-00-00 |
Oxcarbazepine HUMAN PRESCRIPTION DRUG Details:
Item Description | Oxcarbazepine from Sun Pharmaceutical Industries Limited |
LABELER NAME: | Sun Pharmaceutical Industries Limited |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 150(mg/1) |
START MARKETING DATE: | 2007-10-09 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 62756-183_3342c01e-7e6b-434f-b2a5-cb335a237550 |
PRODUCT NDC: | 62756-183 |
APPLICATION NUMBER: | ANDA077794 |
Other OXCARBAZEPINE Pharmaceutical Manufacturers / Labelers: