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: AB
Application Number: A205995
Product Number: 001
Approval Date: May 26, 2017
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information