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Diprolene Af Drug - Diprolene Af The trade name of the product as shown on the labeling. Dosage - CREAM, AUGMENTED; TOPICAL The product dosage form and route separated by a semi-colon. Active Ingredient(s) - Betamethasone Dipropionate Multiple ingredients are in alphabetical order. Strength - EQ 0.05% BASE The potency of the active ingredient(s), Betamethasone Dipropionate. May repeat for multiple part products. Applicant - SCHERING The firm name holding legal responsibility for Diprolene Af. The firm name is condensed to a maximum twenty character unique string. New Drug Application (NDA) Number - 019555 The FDA assigned number to Diprolene Af. Format is nnnnnn. Product Number - 001 The FDA assigned number to identify Diprolene Af. Each strength is a separate product. May repeat for multiple part products. Format is nnn. Therapeutic Equivalence (TE) Code - AB The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products. Approval Date - Apr 27, 1987 The date Diprolene Af was approved as stated in the FDA approval letter to the applicant. The format is Mmm dd, yyyy. Products approved prior to the January 1, 1982 contain the phrase: "Approved prior to Jan 1, 1982". Reference Listed Drug (RLD) - Yes The pioneer or innovator of Diprolene Af. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No. Type - RX The group or category of approved drugs Diprolene Af is in. Format is RX, OTC, DISCN. Applicant Full Name - Schering Corp The full name of the firm holding legal responsibility for the new application of Diprolene Af. Diprolene Af Uticort 0.025% Lotion; Topical Uticort 0.025% Ointment; Topical Betamethasone Dipropionate Eq 0.05% Base Cream, Augmented; Topical Betamethasone Dipropionate Eq 0.05% Base Cream, Augmented; Topical Betamethasone Dipropionate Eq 0.05% Base Cream, Augmented; Topical Betamethasone Dipropionate Eq 0.05% Base Cream, Augmented; Topical Diprolene Eq 0.05% Base Cream, Augmented; Topical Diprolene Af Eq 0.05% Base Cream, Augmented; Topical Uticort 0.025% Cream; Topical Uticort 0.025% Gel; Topical NewDrugInformation