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 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 Description | VALCHLOR from Actelion Pharmaceuticals US, Inc. |
LABELER NAME: | Actelion Pharmaceuticals US, Inc. |
DEA SCHEDULE: |
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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: