PREDNISOLONE
Summary
FDA approved PREDNISOLONE by LANNETT CO INC. ANDA (Generic) approval (Labeling) on 2024-06-05. SOLUTION, ORAL.
Details
Source
Drug Approval
External ID
ANDA040775-13
Action Date
2024-06-05
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
PREDNISOLONE, SOLUTION, ORAL. Application: ANDA040775
Company
Context & Analysis
LANNETT CO INC has 12 FDA actions in our database.
Frequently Asked Questions
How often does LANNETT CO INC have FDA actions?
LANNETT CO INC has 12 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 "ANDA040775-13" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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