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Topicort Drug - Topicort The trade name of the product as shown on the labeling. Dosage - OINTMENT; TOPICAL The product dosage form and route separated by a semi-colon. Active Ingredient(s) - Desoximetasone Multiple ingredients are in alphabetical order. Strength - 0.25% The potency of the active ingredient(s), Desoximetasone. May repeat for multiple part products. Applicant - TARO PHARMS NORTH The firm name holding legal responsibility for Topicort. The firm name is condensed to a maximum twenty character unique string. New Drug Application (NDA) Number - 018763 The FDA assigned number to Topicort. Format is nnnnnn. Product Number - 001 The FDA assigned number to identify Topicort. 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 - Sep 30, 1983 The date Topicort 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 Topicort. 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 Topicort is in. Format is RX, OTC, DISCN. Applicant Full Name - Taro Pharmaceuticals North America Inc The full name of the firm holding legal responsibility for the new application of Topicort. Topicort Topicort 0.05% Ointment; Topical Topicort 0.25% Ointment; Topical Desoximetasone 0.05% Cream; Topical Desoximetasone 0.25% Cream; Topical Topicort 0.25% Cream; Topical Topicort Lp 0.05% Cream; Topical Desoximetasone 0.05% Gel; Topical Topicort 0.05% Gel; Topical Desoximetasone 0.25% Ointment; Topical Desoximetasone 0.25% Ointment; Topical NewDrugInformation