ZENARA FDA Approval ANDA 216202

ANDA 216202

ZENARA

FDA Drug Application

Application #216202

Application Sponsors

ANDA 216202ZENARA

Marketing Status

Prescription001
Prescription002

Application Products

001TABLET;ORALEQ 5MG BASE0PROCHLORPERAZINE MALEATEPROCHLORPERAZINE MALEATE
002TABLET;ORALEQ 10MG BASE0PROCHLORPERAZINE MALEATEPROCHLORPERAZINE MALEATE

FDA Submissions

UNKNOWN; ORIG1AP2022-06-13STANDARD

Submissions Property Types

ORIG1Null15

TE Codes

001PrescriptionAB
002PrescriptionAB

CDER Filings

Accessdata Error
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 216202
            [companyName] => Accessdata Error
            [docInserts] => ["",""]
            [products] => []
            [labels] => 
            [originalApprovals] => []
            [supplements] => 
            [actionDate] => 0000-00-00
        )

)

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