Active Ingredient: MINOXIDIL
Proprietary Name: MINOXIDIL (FOR WOMEN)
Dosage Form; Route of Administration: SOLUTION; TOPICAL
Strength: 2%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074743
Product Number: 001
Approval Date: Oct 18, 1996
Applicant Holder Full Name: SIGHT PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
