PREDNISOLONE SODIUM PHOSPHATE
Summary
FDA approved PREDNISOLONE SODIUM PHOSPHATE by PHARM ASSOC. ANDA (Generic) approval (Labeling) on 2024-06-05. SOLUTION, ORAL.
Details
Source
Drug Approval
External ID
ANDA078988-11
Action Date
2024-06-05
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
PREDNISOLONE SODIUM PHOSPHATE, SOLUTION, ORAL. Application: ANDA078988
Company
Context & Analysis
PHARM ASSOC has 13 FDA actions in our database.
Frequently Asked Questions
How often does PHARM ASSOC have FDA actions?
PHARM ASSOC has 13 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 "ANDA078988-11" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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