Teflaro (Forest Laboratories, Inc.)


Welcome to the PulseAid listing for the Teflaro drug offered from Forest Laboratories, Inc.. This Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] 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: Forest Laboratories, Inc.
NON-PROPRIETARY NAME: ceftaroline fosamil
SUBSTANCE NAME: CEFTAROLINE FOSAMIL
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]
ROUTE: INTRAVENOUS
DOSAGE FORM: POWDER, FOR SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2010-10-29
END MARKETING DATE: 0000-00-00


Teflaro HUMAN PRESCRIPTION DRUG Details:

Item DescriptionTeflaro from Forest Laboratories, Inc.
LABELER NAME: Forest Laboratories, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 400(mg/20mL)
START MARKETING DATE: 2010-10-29
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0456-0400_8f284a4d-916c-4396-bccc-b6481e8b9502
PRODUCT NDC: 0456-0400
APPLICATION NUMBER: NDA200327

Other CEFTAROLINE FOSAMIL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Forest Laboratories, Inc.Teflaro