Application Sponsors
Marketing Status
Application Products
001 | INJECTABLE;INJECTION | 20MG/ML | 0 | DOXAPRAM HYDROCHLORIDE | DOXAPRAM HYDROCHLORIDE |
FDA Submissions
| ORIG | 1 | AP | 2003-01-10 | |
LABELING; Labeling | SUPPL | 2 | AP | 2007-05-29 | |
TE Codes
CDER Filings
ATHENEX INC
cder:Array
(
[0] => Array
(
[ApplNo] => 76266
[companyName] => ATHENEX INC
[docInserts] => ["",""]
[products] => [{"drugName":"DOXAPRAM HYDROCHLORIDE","activeIngredients":"DOXAPRAM HYDROCHLORIDE","strength":"20MG\/ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
[labels] =>
[originalApprovals] => [{"actionDate":"DOXAPRAM HYDROCHLORIDE","submission":"DOXAPRAM HYDROCHLORIDE","actionType":"20MG\/ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Prescription","inserts":"[]","notes":">No"}]
[supplements] =>
[actionDate] => 1969-12-31
)
)