GLENMARK PHARMS LTD FDA Approval ANDA 205267

ANDA 205267

GLENMARK PHARMS LTD

FDA Drug Application

Application #205267

Application Sponsors

ANDA 205267GLENMARK PHARMS LTD

Marketing Status

None (Tentative Approval)001
None (Tentative Approval)002
None (Tentative Approval)003
None (Tentative Approval)004

Application Products

002TABLET;ORAL25MG0MILNACIPRAN HYDROCHLORIDEMILNACIPRAN HYDROCHLORIDE
003TABLET;ORAL50MG0MILNACIPRAN HYDROCHLORIDEMILNACIPRAN HYDROCHLORIDE
004TABLET;ORAL100MG0MILNACIPRAN HYDROCHLORIDEMILNACIPRAN HYDROCHLORIDE

FDA Submissions

UNKNOWN; ORIG1TA2017-03-30STANDARD

CDER Filings

GLENMARK PHARMS LTD
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 205267
            [companyName] => GLENMARK PHARMS LTD
            [docInserts] => ["",""]
            [products] => [{"drugName":"MILNACIPRAN HYDROCHLORIDE","activeIngredients":"MILNACIPRAN HYDROCHLORIDE","strength":"12.5MG","dosageForm":"TABLET;ORAL","marketingStatus":"None (Tentative Approval)","te":"None","rld":"No","rs":"No"},{"drugName":"MILNACIPRAN HYDROCHLORIDE","activeIngredients":"MILNACIPRAN HYDROCHLORIDE","strength":"25MG","dosageForm":"TABLET;ORAL","marketingStatus":"None (Tentative Approval)","te":"None","rld":"No","rs":"No"},{"drugName":"MILNACIPRAN HYDROCHLORIDE","activeIngredients":"MILNACIPRAN HYDROCHLORIDE","strength":"50MG","dosageForm":"TABLET;ORAL","marketingStatus":"None (Tentative Approval)","te":"None","rld":"No","rs":"No"},{"drugName":"MILNACIPRAN HYDROCHLORIDE","activeIngredients":"MILNACIPRAN HYDROCHLORIDE","strength":"100MG","dosageForm":"TABLET;ORAL","marketingStatus":"None (Tentative Approval)","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"03\/30\/2017","submission":"ORIG-1","actionType":"Tentative Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2017-03-30
        )

)

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