Active Ingredient: BETAMETHASONE DIPROPIONATE
Proprietary Name: DIPROSONE
Dosage Form; Route of Administration: LOTION; TOPICAL
Strength: EQ 0.05% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N017781
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SCHERING CORP SUB SCHERING PLOUGH CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information
