Active Ingredient: ACAMPROSATE CALCIUM
Proprietary Name: ACAMPROSATE CALCIUM
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: 333MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A200143
Product Number: 001
Approval Date: Nov 18, 2013
Applicant Holder Full Name: BARR LABORATORIES INC SUB TEVA PHARMACEUTICALS USA
Marketing Status:
Discontinued
Patent and Exclusivity Information
