BAYSHORE PHARMS LLC FDA Approval ANDA 211712

ANDA 211712

BAYSHORE PHARMS LLC

FDA Drug Application

Application #211712

Application Sponsors

ANDA 211712BAYSHORE PHARMS LLC

Marketing Status

Prescription001
Prescription002

Application Products

001TABLET;ORAL5MG0PINDOLOLPINDOLOL
002TABLET;ORAL10MG0PINDOLOLPINDOLOL

FDA Submissions

UNKNOWN; ORIG1AP2019-08-01STANDARD

Submissions Property Types

ORIG1Null15

TE Codes

001PrescriptionAB
002PrescriptionAB

CDER Filings

BAYSHORE PHARMS LLC
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 211712
            [companyName] => BAYSHORE PHARMS LLC
            [docInserts] => ["",""]
            [products] => [{"drugName":"PINDOLOL","activeIngredients":"PINDOLOL","strength":"5MG","dosageForm":"TABLET;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"},{"drugName":"PINDOLOL","activeIngredients":"PINDOLOL","strength":"10MG","dosageForm":"TABLET;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"08\/01\/2019","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2019-08-01
        )

)

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