PREDNISOLONE ACETATE
Summary
FDA approved PREDNISOLONE ACETATE by AMNEAL. ANDA (Generic) approval on 2025-06-11. SUSPENSION/DROPS, OPHTHALMIC.
Details
Source
Drug Approval
External ID
ANDA218256-1
Action Date
2025-06-11
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
PREDNISOLONE ACETATE, SUSPENSION/DROPS, OPHTHALMIC. Application: ANDA218256
Company
Context & Analysis
AMNEAL has 70 FDA actions in our database.
Frequently Asked Questions
How often does AMNEAL have FDA actions?
AMNEAL has 70 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 "ANDA218256-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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