Application Sponsors
ANDA 073168 | YAOPHARMA CO LTD | |
Marketing Status
Application Products
001 | TABLET;ORAL | 40MG | 0 | VERAPAMIL HYDROCHLORIDE | VERAPAMIL HYDROCHLORIDE |
FDA Submissions
| ORIG | 1 | AP | 1992-07-31 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 2 | AP | 1994-01-24 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 3 | AP | 1997-10-27 | |
LABELING; Labeling | SUPPL | 4 | AP | 1998-06-23 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 5 | AP | 1999-05-05 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 6 | AP | 2002-12-09 | |
MANUF (CMC); Manufacturing (CMC) | SUPPL | 7 | AP | 2002-12-16 | |
Submissions Property Types
SUPPL | 1 | Null | 0 |
SUPPL | 2 | Null | 0 |
SUPPL | 3 | Null | 0 |
SUPPL | 5 | Null | 0 |
SUPPL | 6 | Null | 0 |
SUPPL | 7 | Null | 0 |
CDER Filings
YAOPHARMA CO LTD
cder:Array
(
[0] => Array
(
[ApplNo] => 73168
[companyName] => YAOPHARMA CO LTD
[docInserts] => ["",""]
[products] => [{"drugName":"VERAPAMIL HYDROCHLORIDE","activeIngredients":"VERAPAMIL HYDROCHLORIDE","strength":"40MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
[labels] =>
[originalApprovals] => [{"actionDate":"VERAPAMIL HYDROCHLORIDE","submission":"VERAPAMIL HYDROCHLORIDE","actionType":"40MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
[supplements] =>
[actionDate] => 1969-12-31
)
)