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U.S. Department of Health and Human Services

Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Search results from the "OB_Rx" table for query on "020539."

Dosage Form;Route: TABLET;ORAL
Proprietary Name: LAMISIL
Applicant: NOVARTIS
Strength: EQ 250MG BASE
Application Number: N020539
Product Number: 001
Approval Date: May 10, 1996
Reference Listed Drug Yes
TE Code: AB
Patent and Exclusivity Info for this product: View

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FDA/Center for Drug Evaluation and Research
Office of Generic Drugs
Division of Labeling and Program Support
Update Frequency:

Orange Book Data - Monthly
Generic Drug Product Information & Patent Information - Daily
Orange Book Data Updated Through June 2016
Patent and Generic Drug Product Data Last Updated July 26, 2016