Active Ingredient: BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE
Proprietary Name: LOTRISONE
Dosage Form; Route of Administration: LOTION; TOPICAL
Strength: EQ 0.05% BASE;1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N020010
Product Number: 001
Approval Date: Dec 8, 2000
Applicant Holder Full Name: MERCK SHARP AND DOHME CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information
