ANDA 206516

ACTAVIS LLC

FDA Drug Application

Application #206516

Application Sponsors

ANDA 206516

ACTAVIS LLC

Marketing Status

• Prescription: 001

Application Products

001

POWDER;INTRAVENOUS

EQ 50MG BASE/VIAL

0

LEVOLEUCOVORIN CALCIUM

LEVOLEUCOVORIN CALCIUM

FDA Submissions

UNKNOWN;

ORIG

1

AP

2017-02-13

STANDARD

Submissions Property Types

ORIG

1

Null

15

TE Codes

001

Prescription

AP

CDER Filings

ACTAVIS LLC

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 206516
            [companyName] => ACTAVIS LLC
            [docInserts] => ["",""]
            [products] => [{"drugName":"LEVOLEUCOVORIN CALCIUM","activeIngredients":"LEVOLEUCOVORIN CALCIUM","strength":"EQ 50MG BASE\/VIAL","dosageForm":"POWDER;INTRAVENOUS","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"02\/13\/2017","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2017-02-13
        )

)