Amyvid (Eli Lilly and Company)


Welcome to the PulseAid listing for the Amyvid drug offered from Eli Lilly and Company. This Radioactive Diagnostic Agent [EPC],Positron Emitting 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: Eli Lilly and Company
NON-PROPRIETARY NAME: Florbetapir F 18
SUBSTANCE NAME: FLORBETAPIR F-18
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Radioactive Diagnostic Agent [EPC],Positron Emitting Activity [MoA]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2012-06-01
END MARKETING DATE: 0000-00-00


Amyvid HUMAN PRESCRIPTION DRUG Details:

Item DescriptionAmyvid from Eli Lilly and Company
LABELER NAME: Eli Lilly and Company
DEA SCHEDULE:
ACTIVE STRENGTH: 51(mCi/mL)
START MARKETING DATE: 2012-06-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0002-1200_4bd46cbe-cdc1-4329-a8e7-22816bd7fc33
PRODUCT NDC: 0002-1200
APPLICATION NUMBER: NDA202008

Other FLORBETAPIR F-18 Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Eli Lilly and CompanyAmyvid