Active Ingredient: PROCAINAMIDE HYDROCHLORIDE
Proprietary Name: PROCAINAMIDE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 1GM
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040111
Product Number: 001
Approval Date: Dec 13, 1996
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information