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Approved Drug Products containing 21746 listed in the FDA Orange Book. Original Data : FDA Website

FDA Orange Book

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01 1LEES PHARM HK

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01

Brand Name : SURFAXIN

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Brand Name : SURFAXIN

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Not Confirmed
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Dosage Form : SUSPENSION; INTRATRACHEAL

Proprietary Name : SURFAXIN

Dosage Strength : 8.5ML

Approval Date : 2012-03-06

Application Number : 21746

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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