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Approved Drug Products containing 208219 listed in the FDA Orange Book. Original Data : FDA Website

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01 1BAUSCH AND LOMB INC

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Brand Name : LOTEMAX SM

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Brand Name : LOTEMAX SM

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Bausch & Lomb Incorporated

Dosage Form : GEL; OPHTHALMIC

Proprietary Name : LOTEMAX SM

Dosage Strength : 0.38%

Approval Date : 2019-02-22

Application Number : 208219

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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