Active Ingredient: NIACIN
Proprietary Name: NIACIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A076378
Product Number: 001
Approval Date: Apr 26, 2005
Applicant Holder Full Name: BARR LABORATORIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information