Active Ingredient: BUTENAFINE HYDROCHLORIDE
Proprietary Name: MENTAX
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 1%
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N020524
Product Number: 001
Approval Date: Oct 18, 1996
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
