Strength
240 mg/1
Manufacturer
Dr. Reddy's Laboratories Inc.NDC
43598043060
Classification
Generic
Dosage Form
CAPSULE, DELAYED RELEASE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
DIMETHYL FUMARATEApproval Type
Generic (ANDA)
FDA Application
ANDA210460On Market Since
9/25/2020
Related Drugs
Same classification
No related drugs found.