LATANOPROST
Summary
FDA approved LATANOPROST by BAUSCH AND LOMB. ANDA (Generic) approval (Labeling) on 2023-12-27. SOLUTION/DROPS, OPHTHALMIC.
Details
Source
Drug Approval
External ID
ANDA201006-16
Action Date
2023-12-27
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
LATANOPROST, SOLUTION/DROPS, OPHTHALMIC. Application: ANDA201006
Company
Context & Analysis
BAUSCH AND LOMB has 6 FDA actions in our database, including 2 clearances.
Frequently Asked Questions
How often does BAUSCH AND LOMB have FDA actions?
BAUSCH AND LOMB has 6 FDA actions in our database, including 0 recalls and 2 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA201006-16" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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