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Approved Drug Products containing 21081 listed in the FDA Orange Book. Original Data : FDA Website

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01 2SANOFI AVENTIS US

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PharmaCompass

01

Brand Name : LANTUS

Sanofi

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : LANTUS

Dosage Strength : 100 UNITS/ML

Approval Date :

Application Number : 21081

RX/OTC/DISCN :

RLD :

TE Code :

Sanofi Company Banner

02

Brand Name : LANTUS SOLOSTAR

Sanofi

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : LANTUS SOLOSTAR

Dosage Strength : 300 UNITS/3ML (100 UNITS...

Approval Date :

Application Number : 21081

RX/OTC/DISCN :

RLD :

TE Code :

Sanofi Company Banner