ZITHRANOL-RR (Elorac Inc.)


Welcome to the PulseAid listing for the ZITHRANOL-RR drug offered from Elorac 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: Elorac Inc.
NON-PROPRIETARY NAME: anthralin
SUBSTANCE NAME: ANTHRALIN
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2009-07-09
END MARKETING DATE: 0000-00-00


ZITHRANOL-RR HUMAN PRESCRIPTION DRUG Details:

Item DescriptionZITHRANOL-RR from Elorac Inc.
LABELER NAME: Elorac Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 0.012(g/g)
START MARKETING DATE: 2009-07-09
END MARKETING DATE: 0000-00-00
PRODUCT ID: 42783-101_9910c570-35f6-4748-bce0-a4cfb99f7af3
PRODUCT NDC: 42783-101
APPLICATION NUMBER:

Other ANTHRALIN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Elorac Inc.ZITHRANOL-RR
Summers Laboratories IncDRITHO-CREME