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:
Application Number: A077714
Product Number: 001
Approval Date: Jun 4, 2010
Applicant Holder Full Name: BRECKENRIDGE PHARMACEUTICAL INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
