Primidone (Dr. Reddy’s Laboratories Ltd)
Welcome to the PulseAid listing for the Primidone drug offered from Dr. Reddy’s Laboratories Ltd. 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: | Dr. Reddy’s Laboratories Ltd |
NON-PROPRIETARY NAME: | Primidone |
SUBSTANCE NAME: | PRIMIDONE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2008-10-03 |
END MARKETING DATE: | 0000-00-00 |
Primidone HUMAN PRESCRIPTION DRUG Details:
Item Description | Primidone from Dr. Reddy’s Laboratories Ltd |
LABELER NAME: | Dr. Reddy’s Laboratories Ltd |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 250(mg/1) |
START MARKETING DATE: | 2008-10-03 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 55111-476_59ee4631-0d3f-26a9-6b7a-5f265d6298ea |
PRODUCT NDC: | 55111-476 |
APPLICATION NUMBER: | ANDA040862 |
Other PRIMIDONE Pharmaceutical Manufacturers / Labelers: