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Approved Drug Products containing 216151 listed in the FDA Orange Book. Original Data : FDA Website

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01 1NOVITIUM PHARMA

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Brand Name : LACOSAMIDE

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Brand Name : LACOSAMIDE

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Novitium Pharma LLC

Dosage Form : SOLUTION; ORAL

Proprietary Name : LACOSAMIDE

Dosage Strength : 10MG/ML

Approval Date : 2022-08-26

Application Number : 216151

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

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