Active Ingredient: IMIQUIMOD
Proprietary Name: ALDARA
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N020723
Product Number: 001
Approval Date: Feb 27, 1997
Applicant Holder Full Name: BAUSCH HEALTH US LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information