DIMETHYL FUMARATE
Summary
FDA approved DIMETHYL FUMARATE by AUROBINDO PHARMA. ANDA (Generic) approval (Labeling) on 2024-12-17. CAPSULE, DELAYED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA210385-5
Action Date
2024-12-17
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
DIMETHYL FUMARATE, CAPSULE, DELAYED RELEASE, ORAL. Application: ANDA210385
Company
Context & Analysis
AUROBINDO PHARMA has 76 FDA actions in our database.
Frequently Asked Questions
How often does AUROBINDO PHARMA have FDA actions?
AUROBINDO PHARMA has 76 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 "ANDA210385-5" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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