Active Ingredient: QUINIDINE SULFATE
Proprietary Name: QUINIDINE SULFATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A084914
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SANDOZ INC
Marketing Status:
Discontinued
Patent and Exclusivity Information