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FDA Drug Approval, N008816, XYLOCAINE
FDA Drug Approval, N008816, XYLOCAINE
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NDA: 008816
Company: EPIC PHARMA LLC
Drug Name: XYLOCAINE
Active Ingredients: LIDOCAINE HYDROCHLORIDE
Strength: 2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage Form/Route: JELLY;TOPICAL
Action Date: 03/12/1953
Marketing Status: Discontinued
Submission Classification: Type 3 - New Dosage Form
Company: EPIC PHARMA LLC
Drug Name: XYLOCAINE
Active Ingredients: LIDOCAINE HYDROCHLORIDE
Strength: 2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage Form/Route: JELLY;TOPICAL
Action Date: 03/12/1953
Marketing Status: Discontinued
Submission Classification: Type 3 - New Dosage Form
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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