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 Description | Amyvid from Eli Lilly and Company |
LABELER NAME: | Eli Lilly and Company |
DEA SCHEDULE: |
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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: