Celontin (Parke-Davis Div of Pfizer Inc)
Welcome to the PulseAid listing for the Celontin drug offered from Parke-Davis Div of Pfizer 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: | Parke-Davis Div of Pfizer Inc |
NON-PROPRIETARY NAME: | methsuximide |
SUBSTANCE NAME: | METHSUXIMIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1957-02-08 |
END MARKETING DATE: | 0000-00-00 |
Celontin HUMAN PRESCRIPTION DRUG Details:
Item Description | Celontin from Parke-Davis Div of Pfizer Inc |
LABELER NAME: | Parke-Davis Div of Pfizer Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 300(mg/1) |
START MARKETING DATE: | 1957-02-08 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0071-0525_fe1649b6-8f71-467b-aad4-275615657668 |
PRODUCT NDC: | 0071-0525 |
APPLICATION NUMBER: | NDA010596 |
Other METHSUXIMIDE Pharmaceutical Manufacturers / Labelers: