FLAVALTA (LIDOCAINE HYDROCHLORIDE AND EPINEPHRINE)
Summary
FDA approved FLAVALTA (LIDOCAINE HYDROCHLORIDE AND EPINEPHRINE) by DEPROCO. NDA (New Drug) approval (Type 5 - New Formulation or New Manufacturer) on 2026-03-19. SOLUTION, INJECTION.
Details
Source
Drug Approval
External ID
NDA216564-1
Action Date
2026-03-19
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
FLAVALTA (generic: LIDOCAINE HYDROCHLORIDE AND EPINEPHRINE), SOLUTION, INJECTION. Application: NDA216564
Company
Context & Analysis
Frequently Asked Questions
How often does DEPROCO have FDA actions?
This is the only FDA action we have on record for DEPROCO in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA216564-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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