PREDNISONE
Summary
FDA approved PREDNISONE by WATSON LABS. ANDA (Generic) approval (Labeling) on 2024-06-05. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA085162-85
Action Date
2024-06-05
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
PREDNISONE, TABLET, ORAL. Application: ANDA085162
Company
Context & Analysis
WATSON LABS has 30 FDA actions in our database.
Frequently Asked Questions
How often does WATSON LABS have FDA actions?
WATSON LABS has 30 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 "ANDA085162-85" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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