NDA 018184

B BRAUN

FDA Drug Application

Application #018184

Application Sponsors

NDA 018184

B BRAUN

Marketing Status

• Discontinued: 001

Application Products

001

INJECTABLE;INJECTION

450MG/100ML

0

SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER

SODIUM CHLORIDE

FDA Submissions

	ORIG	1	AP	1979-06-08
LABELING; Labeling	SUPPL	2	AP	1979-10-16
MANUF (CMC); Manufacturing (CMC)	SUPPL	3	AP	1980-02-12
MANUF (CMC); Manufacturing (CMC)	SUPPL	4	AP	1980-08-06
MANUF (CMC); Manufacturing (CMC)	SUPPL	5	AP	1980-10-24
LABELING; Labeling	SUPPL	6	AP	1983-01-24
MANUF (CMC); Manufacturing (CMC)	SUPPL	7	AP	1981-10-26
MANUF (CMC); Manufacturing (CMC)	SUPPL	8	AP	1986-02-18
MANUF (CMC); Manufacturing (CMC)	SUPPL	9	AP	1985-06-28
MANUF (CMC); Manufacturing (CMC)	SUPPL	10	AP	1985-04-03
LABELING; Labeling	SUPPL	11	AP	1985-06-04
MANUF (CMC); Manufacturing (CMC)	SUPPL	12	AP	1987-12-30
MANUF (CMC); Manufacturing (CMC)	SUPPL	14	AP	1990-09-11
LABELING; Labeling	SUPPL	15	AP	1991-12-02

Submissions Property Types

ORIG	1	Null	0
SUPPL	2	Null	0
SUPPL	3	Null	0
SUPPL	4	Null	0
SUPPL	5	Null	0
SUPPL	6	Null	0
SUPPL	7	Null	0
SUPPL	8	Null	0
SUPPL	9	Null	0
SUPPL	10	Null	0
SUPPL	11	Null	0
SUPPL	12	Null	0
SUPPL	14	Null	0
SUPPL	15	Null	0

CDER Filings

B BRAUN

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 18184
            [companyName] => B BRAUN
            [docInserts] => ["",""]
            [products] => [{"drugName":"SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER","activeIngredients":"SODIUM CHLORIDE","strength":"450MG\/100ML","dosageForm":"INJECTABLE;INJECTION","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER","submission":"SODIUM CHLORIDE","actionType":"450MG\/100ML","submissionClassification":"INJECTABLE;INJECTION","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)