Active Ingredient: CLOTRIMAZOLE
Proprietary Name: LOTRIMIN
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N017619
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SCHERING PLOUGH HEALTHCARE PRODUCTS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information