Active Ingredient: ACAMPROSATE CALCIUM
Proprietary Name: CAMPRAL
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: 333MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N021431
Product Number: 001
Approval Date: Jul 29, 2004
Applicant Holder Full Name: FOREST LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
