ANDA 087930

CHARTWELL RX

FDA Drug Application

Application #087930

Application Sponsors

ANDA 087930

CHARTWELL RX

Marketing Status

• Discontinued: 001

Application Products

001

CAPSULE;ORAL

37.5MG

0

PHENTERMINE HYDROCHLORIDE

PHENTERMINE HYDROCHLORIDE

FDA Submissions

	ORIG	1	AP	1983-10-14
MANUF (CMC); Manufacturing (CMC)	SUPPL	5	AP	1988-06-27
MANUF (CMC); Manufacturing (CMC)	SUPPL	6	AP	1988-06-27
MANUF (CMC); Manufacturing (CMC)	SUPPL	7	AP	1989-05-31
LABELING; Labeling	SUPPL	8	AP	1989-05-02
MANUF (CMC); Manufacturing (CMC)	SUPPL	10	AP	1992-10-16
LABELING; Labeling	SUPPL	11	AP	1997-12-19
LABELING; Labeling	SUPPL	12	AP	1998-04-08
LABELING; Labeling	SUPPL	13	AP	1998-08-19
LABELING; Labeling	SUPPL	14	AP	1998-11-03
MANUF (CMC); Manufacturing (CMC)	SUPPL	16	AP	2000-10-06

Submissions Property Types

SUPPL	5	Null	0
SUPPL	6	Null	0
SUPPL	7	Null	0
SUPPL	10	Null	0
SUPPL	16	Null	0

CDER Filings

CHARTWELL RX

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 87930
            [companyName] => CHARTWELL RX
            [docInserts] => ["",""]
            [products] => [{"drugName":"PHENTERMINE HYDROCHLORIDE","activeIngredients":"PHENTERMINE HYDROCHLORIDE","strength":"37.5MG","dosageForm":"CAPSULE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"PHENTERMINE HYDROCHLORIDE","submission":"PHENTERMINE HYDROCHLORIDE","actionType":"37.5MG","submissionClassification":"CAPSULE;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)