Active Ingredient: QUINIDINE GLUCONATE
Proprietary Name: QUINIDINE GLUCONATE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 324MG
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A089338
Product Number: 001
Approval Date: Feb 11, 1987
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information