PREDNISOLONE
Summary
FDA approved PREDNISOLONE by AUROBINDO PHARMA LTD. ANDA (Generic) approval (Labeling) on 2024-06-05. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA215673-1
Action Date
2024-06-05
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
PREDNISOLONE, TABLET, ORAL. Application: ANDA215673
Company
Context & Analysis
AUROBINDO PHARMA LTD has 77 FDA actions in our database.
Frequently Asked Questions
How often does AUROBINDO PHARMA LTD have FDA actions?
AUROBINDO PHARMA LTD has 77 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 "ANDA215673-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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