DIMETHYL FUMARATE
Summary
FDA approved DIMETHYL FUMARATE by SOLA PHARMS. ANDA (Generic) approval (Labeling) on 2024-12-18. CAPSULE, DELAYED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA210436-2
Action Date
2024-12-18
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
DIMETHYL FUMARATE, CAPSULE, DELAYED RELEASE, ORAL. Application: ANDA210436
Company
Context & Analysis
SOLA PHARMS has 2 FDA actions in our database.
Frequently Asked Questions
How often does SOLA PHARMS have FDA actions?
SOLA PHARMS has 2 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 "ANDA210436-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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