LILLY FDA Approval NDA 010012

NDA 010012

LILLY

FDA Drug Application

Application #010012

Application Sponsors

NDA 010012LILLY

Marketing Status

Discontinued001

Application Products

001INJECTABLE;INJECTION2.5MG/ML0SANDRILRESERPINE

FDA Submissions

MANUF (CMC); Manufacturing (CMC)SUPPL4AP1981-10-22STANDARD
LABELING; LabelingSUPPL6AP1983-07-20

Submissions Property Types

SUPPL4Null0

CDER Filings

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 10012
            [companyName] => 
            [docInserts] => ["",""]
            [products] => []
            [labels] => 
            [originalApprovals] => []
            [supplements] => 
            [actionDate] => 0000-00-00
        )

)

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