Pomalyst (Celgene Corporation)


Welcome to the PulseAid listing for the Pomalyst drug offered from Celgene Corporation. This Thalidomide Analog [EPC] 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: Celgene Corporation
NON-PROPRIETARY NAME: pomalidomide
SUBSTANCE NAME: POMALIDOMIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Thalidomide Analog [EPC]
ROUTE: ORAL
DOSAGE FORM: CAPSULE
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2013-02-18
END MARKETING DATE: 0000-00-00


Pomalyst HUMAN PRESCRIPTION DRUG Details:

Item DescriptionPomalyst from Celgene Corporation
LABELER NAME: Celgene Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 1(mg/1)
START MARKETING DATE: 2013-02-18
END MARKETING DATE: 0000-00-00
PRODUCT ID: 59572-501_3c66b053-0cf9-4404-9ab4-301867433b8e
PRODUCT NDC: 59572-501
APPLICATION NUMBER: NDA204026

Other POMALIDOMIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Celgene CorporationPomalyst