Chenodal (Retrophin, Inc.)


Welcome to the PulseAid listing for the Chenodal drug offered from Retrophin, Inc.. This 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: Retrophin, Inc.
NON-PROPRIETARY NAME: Chenodiol
SUBSTANCE NAME: CHENODIOL
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2015-12-28
END MARKETING DATE: 0000-00-00


Chenodal HUMAN PRESCRIPTION DRUG Details:

Item DescriptionChenodal from Retrophin, Inc.
LABELER NAME: Retrophin, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 250(mg/1)
START MARKETING DATE: 2015-12-28
END MARKETING DATE: 0000-00-00
PRODUCT ID: 68974-876_277566fc-6896-45e7-913d-b7a74291f07f
PRODUCT NDC: 68974-876
APPLICATION NUMBER: ANDA091019

Other CHENODIOL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Manchester Pharmaceuticals Inc.Chenodal
Nexgen Pharma, Inc.Chenodiol
Retrophin, Inc.Chenodal