ANDA 085517

ABBOTT

FDA Drug Application

Application #085517

Application Sponsors

ANDA 085517

ABBOTT

Marketing Status

• Discontinued: 001

Application Products

001

CAPSULE;ORAL

5MG

0

A-POXIDE

CHLORDIAZEPOXIDE HYDROCHLORIDE

FDA Submissions

	ORIG	1	AP	1977-07-01
MANUF (CMC); Manufacturing (CMC)	SUPPL	6	AP	1982-03-31
MANUF (CMC); Manufacturing (CMC)	SUPPL	7	AP	1982-03-31
MANUF (CMC); Manufacturing (CMC)	SUPPL	9	AP	1984-01-25

Submissions Property Types

SUPPL	6	Null	0
SUPPL	7	Null	0
SUPPL	9	Null	0

CDER Filings

ABBOTT

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 85517
            [companyName] => ABBOTT
            [docInserts] => ["",""]
            [products] => [{"drugName":"A-POXIDE","activeIngredients":"CHLORDIAZEPOXIDE HYDROCHLORIDE","strength":"5MG","dosageForm":"CAPSULE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"A-POXIDE","submission":"CHLORDIAZEPOXIDE HYDROCHLORIDE","actionType":"5MG","submissionClassification":"CAPSULE;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)