Curosurf (Chiesi USA, Inc.)


Welcome to the PulseAid listing for the Curosurf drug offered from Chiesi USA, Inc.. This Alveolar Surface Tension Reduction [PE],Surfactant [EPC],Surfactant Activity [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: Chiesi USA, Inc.
NON-PROPRIETARY NAME: poractant alfa
SUBSTANCE NAME: PORACTANT ALFA
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Alveolar Surface Tension Reduction [PE],Surfactant [EPC],Surfactant Activity [MoA]
ROUTE: ENDOTRACHEAL
DOSAGE FORM: SUSPENSION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1999-11-18
END MARKETING DATE: 0000-00-00


Curosurf HUMAN PRESCRIPTION DRUG Details:

Item DescriptionCurosurf from Chiesi USA, Inc.
LABELER NAME: Chiesi USA, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 80(mg/mL)
START MARKETING DATE: 1999-11-18
END MARKETING DATE: 0000-00-00
PRODUCT ID: 10122-510_7877d4dd-0042-4fb6-b467-dfd4f0d4e31e
PRODUCT NDC: 10122-510
APPLICATION NUMBER: NDA020744

Other PORACTANT ALFA Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Chiesi USA, Inc.Curosurf