$TLGT FDA Approval of Desonide topical ointment?!? https://www.accessdata.fda.gov/scripts/cder/ob/results_product.cfm?Appl_Type=A&Appl_No=212002 Product Details for ANDA 212002 DESONIDE (DESONIDE) 0.05% Marketing Status: Prescription Active Ingredient: DESONIDE Proprietary Name: DESONIDE Dosage Form; Route of Administration: OINTMENT; TOPICAL Strength: 0.05% Reference Listed Drug: No Reference Standard: No TE Code: AB Application Number: A212002 Product Number: 001 Approval Date: Mar 12, 2019 Applicant Holder Full Name: TELIGENT PHARMA INC Marketing Status: Prescription Patent and Exclusivity Information GLTA!!