ANDA 070999

FUTURE PAK

FDA Drug Application

Application #070999

Application Sponsors

ANDA 070999

FUTURE PAK

Marketing Status

• Discontinued: 001

Application Products

001

TABLET, EXTENDED RELEASE;ORAL

10MEQ

0

K+10

POTASSIUM CHLORIDE

FDA Submissions

	ORIG	1	AP	1987-10-22
BIOEQUIV; Bioequivalence	SUPPL	4	AP	1992-11-16
MANUF (CMC); Manufacturing (CMC)	SUPPL	5	AP	1994-07-22
MANUF (CMC); Manufacturing (CMC)	SUPPL	6	AP	1995-06-23
MANUF (CMC); Manufacturing (CMC)	SUPPL	7	AP	1995-06-23

Submissions Property Types

SUPPL	4	Null	0
SUPPL	5	Null	0
SUPPL	6	Null	0
SUPPL	7	Null	0

CDER Filings

FUTURE PAK

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 70999
            [companyName] => FUTURE PAK
            [docInserts] => ["",""]
            [products] => [{"drugName":"K+10","activeIngredients":"POTASSIUM CHLORIDE","strength":"10MEQ","dosageForm":"TABLET, EXTENDED RELEASE;ORAL","marketingStatus":"Discontinued","te":"None","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"K+10","submission":"POTASSIUM CHLORIDE","actionType":"10MEQ","submissionClassification":"TABLET, EXTENDED RELEASE;ORAL","reviewPriority":"Discontinued","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 2020-11-07
        )

)