LIDOCAINE (LIDOCAINE HYDROCHLORIDE)
Summary
FDA approved LIDOCAINE (LIDOCAINE HYDROCHLORIDE) by SENTISS. ANDA (Generic) approval (Manufacturing (CMC)) on 2025-08-27. JELLY, TOPICAL.
Details
Source
Drug Approval
External ID
ANDA040433-20
Action Date
2025-08-27
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
LIDOCAINE (generic: LIDOCAINE HYDROCHLORIDE), JELLY, TOPICAL. Application: ANDA040433
Company
Context & Analysis
SENTISS has 2 FDA actions in our database.
Frequently Asked Questions
How often does SENTISS have FDA actions?
SENTISS has 2 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA040433-20" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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