GLENMARK PHARMS LTD FDA Approval ANDA 206597

ANDA 206597

GLENMARK PHARMS LTD

FDA Drug Application

Application #206597

Application Sponsors

ANDA 206597GLENMARK PHARMS LTD

Marketing Status

Prescription001

Application Products

001TABLET;ORAL-280.02MG;1MG0HAILEY FE 1/20ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

FDA Submissions

UNKNOWN; ORIG1AP2017-11-21STANDARD

Submissions Property Types

ORIG1Null7

TE Codes

001PrescriptionAB

CDER Filings

Accessdata Error
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 206597
            [companyName] => Accessdata Error
            [docInserts] => ["",""]
            [products] => []
            [labels] => 
            [originalApprovals] => []
            [supplements] => 
            [actionDate] => 0000-00-00
        )

)

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