ANDA 074800

ACTAVIS MID ATLANTIC

FDA Drug Application

Application #074800

Documents

• Review: 2001-07-26

Application Sponsors

ANDA 074800

ACTAVIS MID ATLANTIC

Marketing Status

• Discontinued: 001

Application Products

001

SPRAY, METERED;NASAL

5.2MG/SPRAY

0

CROMOLYN SODIUM

CROMOLYN SODIUM

FDA Submissions

ORIG

1

AP

2001-07-26

CDER Filings

ACTAVIS MID ATLANTIC

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 74800
            [companyName] => ACTAVIS MID ATLANTIC
            [docInserts] => ["",""]
            [products] => [{"drugName":"CROMOLYN SODIUM","activeIngredients":"CROMOLYN SODIUM","strength":"5.2MG\/SPRAY","dosageForm":"SPRAY, METERED;NASAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"CROMOLYN SODIUM","submission":"CROMOLYN SODIUM","actionType":"5.2MG\/SPRAY","submissionClassification":"SPRAY, METERED;NASAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)