ANDA 070549

WATSON LABS TEVA

FDA Drug Application

Application #070549

Application Sponsors

ANDA 070549

WATSON LABS TEVA

Marketing Status

• Discontinued: 001

Application Products

001

TABLET;ORAL

20MG

0

PROPRANOLOL HYDROCHLORIDE

PROPRANOLOL HYDROCHLORIDE

FDA Submissions

	ORIG	1	AP	1986-04-11
LABELING; Labeling	SUPPL	4	AP	1988-11-29
LABELING; Labeling	SUPPL	5	AP	1990-02-28
LABELING; Labeling	SUPPL	6	AP	1990-07-26
LABELING; Labeling	SUPPL	7	AP	1990-09-10
LABELING; Labeling	SUPPL	11	AP	1991-02-04
LABELING; Labeling	SUPPL	12	AP	1992-06-04
LABELING; Labeling	SUPPL	13	AP	1999-02-09
MANUF (CMC); Manufacturing (CMC)	SUPPL	14	AP	1999-11-10
LABELING; Labeling	SUPPL	15	AP	1999-11-17

Submissions Property Types

SUPPL	1	Null	0
SUPPL	14	Null	0

CDER Filings

WATSON LABS TEVA

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 70549
            [companyName] => WATSON LABS TEVA
            [docInserts] => ["",""]
            [products] => [{"drugName":"PROPRANOLOL HYDROCHLORIDE","activeIngredients":"PROPRANOLOL HYDROCHLORIDE","strength":"20MG","dosageForm":"TABLET;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"PROPRANOLOL HYDROCHLORIDE","submission":"PROPRANOLOL HYDROCHLORIDE","actionType":"20MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)