TIAGABINE HYDROCHLORIDE (Sun Pharmaceutical Industries Limited)
Welcome to the PulseAid listing for the TIAGABINE HYDROCHLORIDE 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: | TIAGABINE HYDROCHLORIDE |
| SUBSTANCE NAME: | TIAGABINE HYDROCHLORIDE |
| 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: | 2011-11-04 |
| END MARKETING DATE: | 0000-00-00 |
TIAGABINE HYDROCHLORIDE HUMAN PRESCRIPTION DRUG Details:
| Item Description | TIAGABINE HYDROCHLORIDE from Sun Pharmaceutical Industries Limited |
| LABELER NAME: | Sun Pharmaceutical Industries Limited |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 2(mg/1) |
| START MARKETING DATE: | 2011-11-04 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 62756-200_4ddc4028-7507-4f27-acaf-6f20c6cdc8b1 |
| PRODUCT NDC: | 62756-200 |
| APPLICATION NUMBER: | ANDA077555 |
Other TIAGABINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
