REVONTO (DANTROLENE SODIUM)
Summary
FDA approved REVONTO (DANTROLENE SODIUM) by USWM. ANDA (Generic) approval (Labeling) on 2024-11-22. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
ANDA078378-21
Action Date
2024-11-22
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
REVONTO (generic: DANTROLENE SODIUM), INJECTABLE, INJECTION. Application: ANDA078378
Company
Context & Analysis
Frequently Asked Questions
How often does USWM have FDA actions?
This is the only FDA action we have on record for USWM in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA078378-21" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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