Active Ingredient: TOLTERODINE TARTRATE
Proprietary Name: TOLTERODINE TARTRATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A077006
Product Number: 001
Approval Date: Feb 23, 2015
Applicant Holder Full Name: IVAX PHARMACEUTICALS INC SUB TEVA PHARMACEUTICALS USA
Marketing Status:
Prescription
Patent and Exclusivity Information
