ANDA 213467

GRANULES

FDA Drug Application

Application #213467

Application Sponsors

ANDA 213467

GRANULES

Marketing Status

• Prescription: 001

Application Products

001

FOR SOLUTION;ORAL

20MEQ

0

POTASSIUM CHLORIDE

POTASSIUM CHLORIDE

FDA Submissions

UNKNOWN;

ORIG

1

AP

2022-01-27

STANDARD

Submissions Property Types

ORIG

1

Null

7

TE Codes

001

Prescription

AA

CDER Filings

GRANULES

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 213467
            [companyName] => GRANULES
            [docInserts] => ["",""]
            [products] => [{"drugName":"POTASSIUM CHLORIDE","activeIngredients":"POTASSIUM CHLORIDE","strength":"20MEQ","dosageForm":"FOR SOLUTION;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"01\/27\/2022","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2022-01-27
        )

)