BAUSCH AND LOMB FDA Approval ANDA 090037

ANDA 090037

BAUSCH AND LOMB

FDA Drug Application

Application #090037

Application Sponsors

ANDA 090037BAUSCH AND LOMB

Marketing Status

Prescription001

Application Products

001SOLUTION/DROPS;OPHTHALMICEQ 2% BASE;EQ 0.5% BASE0DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATEDORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE

FDA Submissions

ORIG1AP2009-07-14
LABELING; LabelingSUPPL6AP2013-02-20STANDARD

Submissions Property Types

SUPPL6Null15

TE Codes

001PrescriptionAT

CDER Filings

BAUSCH AND LOMB
cder:Array
(
    [0] => Array
        (
            [ApplNo] => 90037
            [companyName] => BAUSCH AND LOMB
            [docInserts] => ["",""]
            [products] => [{"drugName":"DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE","activeIngredients":"DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE","strength":"EQ 2% BASE;EQ 0.5% BASE","dosageForm":"SOLUTION\/DROPS;OPHTHALMIC","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE","submission":"DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE","actionType":"EQ 2% BASE;EQ 0.5% BASE","submissionClassification":"SOLUTION\/DROPS;OPHTHALMIC","reviewPriority":"Prescription","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)

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