Letairis (Gilead Sciences, Inc)


Welcome to the PulseAid listing for the Letairis drug offered from Gilead Sciences, Inc. This Endothelin Receptor Antagonist [EPC],Endothelin Receptor Antagonists [MoA] 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: Gilead Sciences, Inc
NON-PROPRIETARY NAME: AMBRISENTAN
SUBSTANCE NAME: AMBRISENTAN
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Endothelin Receptor Antagonist [EPC],Endothelin Receptor Antagonists [MoA]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2007-06-15
END MARKETING DATE: 0000-00-00


Letairis HUMAN PRESCRIPTION DRUG Details:

Item DescriptionLetairis from Gilead Sciences, Inc
LABELER NAME: Gilead Sciences, Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 5(mg/1)
START MARKETING DATE: 2007-06-15
END MARKETING DATE: 0000-00-00
PRODUCT ID: 61958-0801_bb56fca3-fff9-4212-ba49-4959ad5a269e
PRODUCT NDC: 61958-0801
APPLICATION NUMBER: NDA022081

Other AMBRISENTAN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Gilead Sciences, IncLetairis