Active Ingredient: IMIQUIMOD
Proprietary Name: IMIQUIMOD
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 5%
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A201994
Product Number: 001
Approval Date: Mar 6, 2012
Applicant Holder Full Name: GLENMARK PHARMACEUTICALS INC USA
Marketing Status:
Prescription
Patent and Exclusivity Information