Active Ingredient: TICLOPIDINE HYDROCHLORIDE
Proprietary Name: TICLOPIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A075526
Product Number: 001
Approval Date: Sep 26, 2002
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information