LOFEXIDINE
Summary
FDA approved LOFEXIDINE by NOVITIUM PHARMA. ANDA (Generic) approval on 2025-10-22. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA219917-1
Action Date
2025-10-22
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
LOFEXIDINE, TABLET, ORAL. Application: ANDA219917
Company
Context & Analysis
NOVITIUM PHARMA has 23 FDA actions in our database.
Frequently Asked Questions
How often does NOVITIUM PHARMA have FDA actions?
NOVITIUM PHARMA has 23 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 "ANDA219917-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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