Strength
333 mg/1
Manufacturer
Major PharmaceuticalsNDC
00904721304
Classification
Generic
Dosage Form
TABLET, DELAYED RELEASE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
ACAMPROSATE CALCIUMApproval Type
Generic (ANDA)
FDA Application
ANDA202229On Market Since
7/16/2013
Related Drugs
Same classification
No related drugs found.