WATSON LABS INC FDA Approval ANDA 074349

ANDA 074349

WATSON LABS INC

FDA Drug Application

Application #074349

Application Sponsors

ANDA 074349WATSON LABS INC

Marketing Status

Discontinued001
Discontinued002
Discontinued003

Application Products

001TABLET;ORAL200MG0CIMETIDINECIMETIDINE
002TABLET;ORAL300MG0CIMETIDINECIMETIDINE
003TABLET;ORAL400MG0CIMETIDINECIMETIDINE

FDA Submissions

ORIG1AP1996-08-30

Submissions Property Types

SUPPL1Null0

CDER Filings

WATSON LABS INC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 74349
            [companyName] => WATSON LABS INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"CIMETIDINE","activeIngredients":"CIMETIDINE","strength":"200MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"CIMETIDINE","activeIngredients":"CIMETIDINE","strength":"300MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"},{"drugName":"CIMETIDINE","activeIngredients":"CIMETIDINE","strength":"400MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"CIMETIDINE","submission":"CIMETIDINE","actionType":"200MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"},{"actionDate":"CIMETIDINE","submission":"CIMETIDINE","actionType":"300MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"},{"actionDate":"CIMETIDINE","submission":"CIMETIDINE","actionType":"400MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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