Active Ingredient: TERBINAFINE HYDROCHLORIDE
Proprietary Name: TERBINAFINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 250MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A076390
Product Number: 001
Approval Date: Jul 2, 2007
Applicant Holder Full Name: DR REDDYS LABORATORIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information
