MOXIFLOXACIN HYDROCHLORIDE
Summary
FDA approved MOXIFLOXACIN HYDROCHLORIDE by SOMERSET THERAPS LLC. ANDA (Generic) approval on 2024-11-14. SOLUTION/DROPS, OPHTHALMIC.
Details
Source
Drug Approval
External ID
ANDA209698-1
Action Date
2024-11-14
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
MOXIFLOXACIN HYDROCHLORIDE, SOLUTION/DROPS, OPHTHALMIC. Application: ANDA209698
Company
Context & Analysis
SOMERSET THERAPS LLC has 26 FDA actions in our database.
Frequently Asked Questions
How often does SOMERSET THERAPS LLC have FDA actions?
SOMERSET THERAPS LLC has 26 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 "ANDA209698-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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