Application Sponsors
Marketing Status
Application Products
001 | INJECTABLE;INJECTION | 40MEQ/100ML | 0 | AMMONIUM CHLORIDE 2.14% | AMMONIUM CHLORIDE |
FDA Submissions
| ORIG | 1 | AP | 1978-10-13 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 3 | AP | 1982-06-04 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 4 | AP | 1983-04-29 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 5 | AP | 1982-12-29 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 9 | AP | 1986-05-05 | |
Submissions Property Types
SUPPL | 3 | Null | 0 |
SUPPL | 4 | Null | 0 |
SUPPL | 5 | Null | 0 |
SUPPL | 9 | Null | 0 |
CDER Filings
B BRAUN
cder:Array
(
[0] => Array
(
[ApplNo] => 85734
[companyName] => B BRAUN
[docInserts] => ["",""]
[products] => [{"drugName":"AMMONIUM CHLORIDE 2.14%","activeIngredients":"AMMONIUM CHLORIDE","strength":"40MEQ\/100ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
[labels] =>
[originalApprovals] => [{"actionDate":"AMMONIUM CHLORIDE 2.14%","submission":"AMMONIUM CHLORIDE","actionType":"40MEQ\/100ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
[supplements] =>
[actionDate] => 1969-12-31
)
)