Application Sponsors
Marketing Status
Application Products
001 | INJECTABLE;INJECTION | EQ 4MG BASE/VIAL | 0 | TOPOTECAN HYDROCHLORIDE | TOPOTECAN HYDROCHLORIDE |
FDA Submissions
| ORIG | 1 | AP | 2010-12-01 | |
LABELING; Labeling | SUPPL | 2 | AP | 2016-02-16 | STANDARD |
LABELING; Labeling | SUPPL | 3 | AP | 2019-09-26 | STANDARD |
LABELING; Labeling | SUPPL | 4 | AP | 2020-08-20 | STANDARD |
Submissions Property Types
ORIG | 1 | Null | 7 |
SUPPL | 2 | Null | 15 |
SUPPL | 3 | Null | 7 |
SUPPL | 4 | Null | 7 |
TE Codes
CDER Filings
CIPLA
cder:Array
(
[0] => Array
(
[ApplNo] => 91199
[companyName] => CIPLA
[docInserts] => ["",""]
[products] => [{"drugName":"TOPOTECAN HYDROCHLORIDE","activeIngredients":"TOPOTECAN HYDROCHLORIDE","strength":"EQ 4MG BASE\/VIAL","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
[labels] =>
[originalApprovals] => [{"actionDate":"TOPOTECAN HYDROCHLORIDE","submission":"TOPOTECAN HYDROCHLORIDE","actionType":"EQ 4MG BASE\/VIAL","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Prescription","inserts":"[]","notes":">No"}]
[supplements] =>
[actionDate] => 1969-12-31
)
)