OXCARBAZEPINE (Breckenridge Pharmaceutical, Inc.)
Welcome to the PulseAid listing for the OXCARBAZEPINE drug offered from Breckenridge Pharmaceutical, 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: | Breckenridge Pharmaceutical, 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: | TABLET, FILM COATED |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2008-01-11 |
| END MARKETING DATE: | 0000-00-00 |
OXCARBAZEPINE HUMAN PRESCRIPTION DRUG Details:
| Item Description | OXCARBAZEPINE from Breckenridge Pharmaceutical, Inc. |
| LABELER NAME: | Breckenridge Pharmaceutical, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 150(mg/1) |
| START MARKETING DATE: | 2008-01-11 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 51991-292_cb6a679d-d9d7-42b0-bd83-ba9c485d0260 |
| PRODUCT NDC: | 51991-292 |
| APPLICATION NUMBER: | ANDA078069 |
Other OXCARBAZEPINE Pharmaceutical Manufacturers / Labelers:
