ATHENEX INC FDA Approval ANDA 075684

ANDA 075684

ATHENEX INC

FDA Drug Application

Application #075684

Documents

Letter2001-04-16
Review2003-07-30

Application Sponsors

ANDA 075684ATHENEX INC

Marketing Status

Prescription001

Application Products

001INJECTABLE;INJECTION10MG/ML0FAMOTIDINEFAMOTIDINE

FDA Submissions

ORIG1AP2001-04-16
LABELING; LabelingSUPPL5AP2008-07-31
LABELING; LabelingSUPPL13AP2022-01-07STANDARD

Submissions Property Types

SUPPL13Null7

TE Codes

001PrescriptionAP

CDER Filings

ATHENEX INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 75684
            [companyName] => ATHENEX INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"FAMOTIDINE","activeIngredients":"FAMOTIDINE","strength":"10MG\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"FAMOTIDINE","submission":"FAMOTIDINE","actionType":"10MG\/ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Prescription","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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