Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 020612

Marketing Status: Prescription
Active Ingredient: LIDOCAINE
Proprietary Name: LIDODERM
Dosage Form; Route of Administration: PATCH; TOPICAL
Strength: 5%
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N020612
Product Number: 001
Approval Date: Mar 19, 1999
Applicant Holder Full Name: TEIKOKU PHARMA USA INC
Marketing Status:  Prescription
Patent and Exclusivity Information

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