DEXAMETHASONE SODIUM PHOSPHATE
Summary
FDA approved DEXAMETHASONE SODIUM PHOSPHATE by AMNEAL. ANDA (Generic) approval (Labeling) on 2024-06-05. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
ANDA208689-7
Action Date
2024-06-05
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
DEXAMETHASONE SODIUM PHOSPHATE, INJECTABLE, INJECTION. Application: ANDA208689
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 "ANDA208689-7" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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