Application Sponsors
Marketing Status
Application Products
001 | TABLET;ORAL | 600MG | 0 | IBU | IBUPROFEN |
FDA Submissions
| ORIG | 1 | AP | 1985-03-29 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 2 | AP | 1986-01-17 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 3 | AP | 1986-01-17 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 4 | AP | 1986-01-17 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 6 | AP | 1986-05-20 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 7 | AP | 1986-05-20 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 9 | AP | 1987-08-27 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 10 | AP | 1987-08-27 | |
LABELING; Labeling | SUPPL | 14 | AP | 1988-02-08 | |
LABELING; Labeling | SUPPL | 15 | AP | 1988-10-07 | |
LABELING; Labeling | SUPPL | 16 | AP | 1989-01-10 | |
LABELING; Labeling | SUPPL | 18 | AP | 1989-10-27 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 19 | AP | 1990-08-16 | |
LABELING; Labeling | SUPPL | 20 | AP | 1991-08-06 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 21 | AP | 1992-08-03 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 22 | AP | 1992-08-03 | |
LABELING; Labeling | SUPPL | 23 | AP | 1991-10-17 | |
LABELING; Labeling | SUPPL | 24 | AP | 1992-03-20 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 26 | AP | 1995-08-11 | |
LABELING; Labeling | SUPPL | 27 | AP | 1995-02-15 | |
Submissions Property Types
ORIG | 1 | Null | 0 |
SUPPL | 2 | Null | 0 |
SUPPL | 3 | Null | 0 |
SUPPL | 4 | Null | 0 |
SUPPL | 5 | Null | 0 |
SUPPL | 6 | Null | 0 |
SUPPL | 7 | Null | 0 |
SUPPL | 9 | Null | 0 |
SUPPL | 10 | Null | 0 |
SUPPL | 14 | Null | 0 |
SUPPL | 15 | Null | 0 |
SUPPL | 16 | Null | 0 |
SUPPL | 18 | Null | 0 |
SUPPL | 19 | Null | 0 |
SUPPL | 20 | Null | 0 |
SUPPL | 21 | Null | 0 |
SUPPL | 22 | Null | 0 |
SUPPL | 23 | Null | 0 |
SUPPL | 24 | Null | 0 |
SUPPL | 26 | Null | 0 |
SUPPL | 27 | Null | 0 |
CDER Filings
BASF
cder:Array
(
[0] => Array
(
[ApplNo] => 70099
[companyName] => BASF
[docInserts] => ["",""]
[products] => [{"drugName":"IBU","activeIngredients":"IBUPROFEN","strength":"600MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
[labels] =>
[originalApprovals] => [{"actionDate":"IBU","submission":"IBUPROFEN","actionType":"600MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
[supplements] =>
[actionDate] => 1969-12-31
)
)