ANDA 075114

ABBVIE

FDA Drug Application

Application #075114

Documents

• Letter: 1999-07-26

Application Sponsors

ANDA 075114

ABBVIE

Marketing Status

• Discontinued: 001

Application Products

001

INJECTABLE;INJECTION

EQ 50MG BASE/ML

0

ACYCLOVIR

ACYCLOVIR SODIUM

FDA Submissions

ORIG

1

AP

1999-07-26

Submissions Property Types

ORIG

1

Null

0

CDER Filings

ABBVIE

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 75114
            [companyName] => ABBVIE
            [docInserts] => ["",""]
            [products] => [{"drugName":"ACYCLOVIR","activeIngredients":"ACYCLOVIR SODIUM","strength":"EQ 50MG BASE\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"ACYCLOVIR","submission":"ACYCLOVIR SODIUM","actionType":"EQ 50MG BASE\/ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)