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Approved Drug Products containing 22244 listed in the FDA Orange Book. Original Data : FDA Website

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01 1EISAI INC

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Brand Name : LUSEDRA

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Brand Name : LUSEDRA

Luxepack
Not Confirmed
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Eisai Inc

Dosage Form : SOLUTION; INTRAVENOUS

Proprietary Name : LUSEDRA

Dosage Strength : 1050MG/30ML (35MG/ML)

Approval Date : 2008-12-12

Application Number : 22244

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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