Prednicarbate (E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.)


Welcome to the PulseAid listing for the Prednicarbate drug offered from E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.. 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: E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
NON-PROPRIETARY NAME: prednicarbate
SUBSTANCE NAME: PREDNICARBATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
ROUTE: TOPICAL
DOSAGE FORM: OINTMENT
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2007-03-09
END MARKETING DATE: 0000-00-00


Prednicarbate HUMAN PRESCRIPTION DRUG Details:

Item DescriptionPrednicarbate from E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
LABELER NAME: E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 1(mg/g)
START MARKETING DATE: 2007-03-09
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0168-0410_9012275c-1ce6-4acb-9889-f652df4f4ad9
PRODUCT NDC: 0168-0410
APPLICATION NUMBER: ANDA077236

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