Application Sponsors
ANDA 213062 | WES PHARMA INC | |
Marketing Status
Prescription | 001 |
Prescription | 002 |
Application Products
001 | SOLUTION;ORAL | 20MEQ/15ML | 0 | POTASSIUM CHLORIDE | POTASSIUM CHLORIDE |
002 | SOLUTION;ORAL | 40MEQ/15ML | 0 | POTASSIUM CHLORIDE | POTASSIUM CHLORIDE |
FDA Submissions
UNKNOWN; | ORIG | 1 | AP | 2022-06-06 | STANDARD |
Submissions Property Types
TE Codes
001 | Prescription | AA |
002 | Prescription | AA |
CDER Filings
WES PHARMA INC
cder:Array
(
[0] => Array
(
[ApplNo] => 213062
[companyName] => WES PHARMA INC
[docInserts] => ["",""]
[products] => [{"drugName":"POTASSIUM CHLORIDE","activeIngredients":"POTASSIUM CHLORIDE","strength":"20MEQ\/15ML","dosageForm":"SOLUTION;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"},{"drugName":"POTASSIUM CHLORIDE","activeIngredients":"POTASSIUM CHLORIDE","strength":"40MEQ\/15ML","dosageForm":"SOLUTION;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
[labels] =>
[originalApprovals] => [{"actionDate":"06\/06\/2022","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
[supplements] =>
[actionDate] => 2022-06-06
)
)