Active Ingredient: QUINIDINE SULFATE
Proprietary Name: QUINIDINE SULFATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A081029
Product Number: 001
Approval Date: Apr 14, 1989
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information