Active Ingredient: ALCLOMETASONE DIPROPIONATE
Proprietary Name: ALCLOMETASONE DIPROPIONATE
Dosage Form; Route of Administration: OINTMENT; TOPICAL
Strength: 0.05%
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A076884
Product Number: 001
Approval Date: Jul 18, 2005
Applicant Holder Full Name: FOUGERA PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information