ANDA 070666

YAOPHARMA CO LTD

FDA Drug Application

Application #070666

Application Sponsors

ANDA 070666

YAOPHARMA CO LTD

Marketing Status

• Discontinued: 001

Application Products

001

TABLET;ORAL

60MG

0

PROPRANOLOL HYDROCHLORIDE

PROPRANOLOL HYDROCHLORIDE

FDA Submissions

	ORIG	1	AP	1986-10-10
LABELING; Labeling	SUPPL	2	AP	1987-03-13
MANUF (CMC); Manufacturing (CMC)	SUPPL	3	AP	1988-12-23
MANUF (CMC); Manufacturing (CMC)	SUPPL	4	AP	1988-12-23
LABELING; Labeling	SUPPL	5	AP	1988-12-23
LABELING; Labeling	SUPPL	6	AP	1987-07-31
MANUF (CMC); Manufacturing (CMC)	SUPPL	7	AP	1988-02-11
MANUF (CMC); Manufacturing (CMC)	SUPPL	9	AP	1988-12-23
MANUF (CMC); Manufacturing (CMC)	SUPPL	10	AP	1988-12-14
LABELING; Labeling	SUPPL	11	AP	1988-11-29
LABELING; Labeling	SUPPL	12	AP	1989-07-10
LABELING; Labeling	SUPPL	13	AP	1992-05-22
MANUF (CMC); Manufacturing (CMC)	SUPPL	14	AP	1995-05-18
MANUF (CMC); Manufacturing (CMC)	SUPPL	15	AP	2001-05-09

Submissions Property Types

SUPPL	1	Null	0
SUPPL	3	Null	0
SUPPL	4	Null	0
SUPPL	7	Null	0
SUPPL	9	Null	0
SUPPL	10	Null	0
SUPPL	14	Null	0
SUPPL	15	Null	0

CDER Filings

YAOPHARMA CO LTD

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 70666
            [companyName] => YAOPHARMA CO LTD
            [docInserts] => ["",""]
            [products] => [{"drugName":"PROPRANOLOL HYDROCHLORIDE","activeIngredients":"PROPRANOLOL HYDROCHLORIDE","strength":"60MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"PROPRANOLOL HYDROCHLORIDE","submission":"PROPRANOLOL HYDROCHLORIDE","actionType":"60MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)