Prednicarbate (Prasco Laboratories)


Welcome to the PulseAid listing for the Prednicarbate drug offered from Prasco Laboratories. This Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] 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: Prasco Laboratories
NON-PROPRIETARY NAME: Prednicarbate
SUBSTANCE NAME: PREDNICARBATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: NDA AUTHORIZED GENERIC
START MARKETING DATE: 2007-04-30
END MARKETING DATE: 0000-00-00


Prednicarbate HUMAN PRESCRIPTION DRUG Details:

Item DescriptionPrednicarbate from Prasco Laboratories
LABELER NAME: Prasco Laboratories
DEA SCHEDULE:
ACTIVE STRENGTH: 1(mg/g)
START MARKETING DATE: 2007-04-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 66993-880_a241f69a-4de4-441a-a3eb-4c9e82d7a5bd
PRODUCT NDC: 66993-880
APPLICATION NUMBER: NDA020279

Other PREDNICARBATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.Prednicarbate
Oceanside PharmaceuticalsPrednicarbate
Prasco LaboratoriesPrednicarbate
Valeant Pharmaceuticals North America LLCDermatop