Active Ingredient: QUINIDINE SULFATE
Proprietary Name: QUINIDEX
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 300MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N012796
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: WYETH PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
