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Approved Drug Products containing 20612 listed in the FDA Orange Book. Original Data : FDA Website

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01 1TEIKOKU PHARMA USA

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Brand Name : LIDODERM

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Brand Name : LIDODERM

Discovery on Target
Not Confirmed
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Teikoku Pharma USA

Dosage Form : PATCH; TOPICAL

Proprietary Name : LIDODERM

Dosage Strength : 5%

Approval Date : 1999-03-19

Application Number : 20612

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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