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 DescriptionCelontin from Parke-Davis Div of Pfizer Inc
LABELER NAME: Parke-Davis Div of Pfizer Inc
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
Parke-Davis Div of Pfizer IncCelontin