Documents
Application Sponsors
Marketing Status
Application Products
001 | TABLET, EXTENDED RELEASE;ORAL | 20MEQ | 0 | POTASSIUM CHLORIDE | POTASSIUM CHLORIDE |
FDA Submissions
| ORIG | 1 | AP | 2002-04-05 | |
LABELING; Labeling | SUPPL | 2 | AP | 2002-10-02 | |
Submissions Property Types
CDER Filings
NESHER PHARMS
cder:Array
(
[0] => Array
(
[ApplNo] => 76044
[companyName] => NESHER PHARMS
[docInserts] => ["",""]
[products] => [{"drugName":"POTASSIUM CHLORIDE","activeIngredients":"POTASSIUM CHLORIDE","strength":"20MEQ","dosageForm":"TABLET, EXTENDED RELEASE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
[labels] =>
[originalApprovals] => [{"actionDate":"POTASSIUM CHLORIDE","submission":"POTASSIUM CHLORIDE","actionType":"20MEQ","submissionClassification":"TABLET, EXTENDED RELEASE;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
[supplements] =>
[actionDate] => 1969-12-31
)
)