VALCHLOR (Actelion Pharmaceuticals US, Inc.)


Welcome to the PulseAid listing for the VALCHLOR drug offered from Actelion Pharmaceuticals US, Inc.. This Alkylating Activity [MoA],Alkylating Drug [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view the 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: Actelion Pharmaceuticals US, Inc.
NON-PROPRIETARY NAME: mechlorethamine hydrochloride
SUBSTANCE NAME: MECHLORETHAMINE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Alkylating Activity [MoA],Alkylating Drug [EPC]
ROUTE: TOPICAL
DOSAGE FORM: GEL
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2013-10-21
END MARKETING DATE: 0000-00-00


VALCHLOR HUMAN PRESCRIPTION DRUG Details:

Item DescriptionVALCHLOR from Actelion Pharmaceuticals US, Inc.
LABELER NAME: Actelion Pharmaceuticals US, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 0.012(g/60g)
START MARKETING DATE: 2013-10-21
END MARKETING DATE: 0000-00-00
PRODUCT ID: 66215-016_ae5a19e4-8f22-4616-ba92-b187d0cdbded
PRODUCT NDC: 66215-016
APPLICATION NUMBER: NDA202317

Other MECHLORETHAMINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Actelion Pharmaceuticals US, Inc.VALCHLOR