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Approved Drug Products containing 207648 listed in the FDA Orange Book. Original Data : FDA Website

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01 4FRESENIUS KABI USA

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01

Brand Name : SMOFLIPID 20%

Discovery on Target
Not Confirmed
arrow

Brand Name : SMOFLIPID 20%

Discovery on Target
Not Confirmed
arrow

Fresenius Kabi USA

Dosage Form : EMULSION; INTRAVENOUS

Proprietary Name : SMOFLIPID 20%

Dosage Strength : 3GM/100ML;6GM/100ML;5GM/...

Approval Date : 2016-07-13

Application Number : 207648

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

blank

02

Brand Name : SMOFLIPID 20%

Discovery on Target
Not Confirmed
arrow

Brand Name : SMOFLIPID 20%

Discovery on Target
Not Confirmed
arrow

Fresenius Kabi USA

Dosage Form : EMULSION; INTRAVENOUS

Proprietary Name : SMOFLIPID 20%

Dosage Strength : 3GM/100ML;6GM/100ML;5GM/...

Approval Date : 2016-07-13

Application Number : 207648

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

blank

03

Brand Name : SMOFLIPID 20%

Discovery on Target
Not Confirmed
arrow

Brand Name : SMOFLIPID 20%

Discovery on Target
Not Confirmed
arrow

Fresenius Kabi USA

Dosage Form : EMULSION; INTRAVENOUS

Proprietary Name : SMOFLIPID 20%

Dosage Strength : 3GM/100ML;6GM/100ML;5GM/...

Approval Date : 2018-08-10

Application Number : 207648

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

blank

04

Brand Name : SMOFLIPID 20%

Discovery on Target
Not Confirmed
arrow

Brand Name : SMOFLIPID 20%

Discovery on Target
Not Confirmed
arrow

Fresenius Kabi USA

Dosage Form : EMULSION; INTRAVENOUS

Proprietary Name : SMOFLIPID 20%

Dosage Strength : 3GM/100ML;6GM/100ML;5GM/...

Approval Date : 2016-07-13

Application Number : 207648

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

blank