Application Sponsors
Marketing Status
Application Products
001 | SOLUTION;ORAL | 100MG/ML | 0 | CYCLOSPORINE | CYCLOSPORINE |
FDA Submissions
| ORIG | 1 | AP | 2001-12-18 | |
LABELING; Labeling | SUPPL | 2 | AP | 2002-05-03 | |
LABELING; Labeling | SUPPL | 3 | AP | 2004-05-14 | |
LABELING; Labeling | SUPPL | 4 | AP | 2004-12-02 | |
LABELING; Labeling | SUPPL | 8 | AP | 2007-02-05 | |
LABELING; Labeling | SUPPL | 10 | AP | 2007-11-16 | |
LABELING; Labeling | SUPPL | 19 | AP | 2015-01-20 | STANDARD |
Submissions Property Types
TE Codes
CDER Filings
MAYNE PHARMA
cder:Array
(
[0] => Array
(
[ApplNo] => 65054
[companyName] => MAYNE PHARMA
[docInserts] => ["",""]
[products] => [{"drugName":"CYCLOSPORINE","activeIngredients":"CYCLOSPORINE","strength":"100MG\/ML","dosageForm":"SOLUTION;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
[labels] =>
[originalApprovals] => [{"actionDate":"CYCLOSPORINE","submission":"CYCLOSPORINE","actionType":"100MG\/ML","submissionClassification":"SOLUTION;ORAL","reviewPriority":"Prescription","inserts":"[]","notes":">No"}]
[supplements] =>
[actionDate] => 1969-12-31
)
)