Triamcinolone Diacetate

   
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Triamcinolone Diacetate


Drug - Triamcinolone Diacetate
The trade name of the product as shown on the labeling.

Dosage - INJECTABLE; INJECTION
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Triamcinolone Diacetate
Multiple ingredients are in alphabetical order.

Strength - 25MG/ML
The potency of the active ingredient(s), Triamcinolone Diacetate. May repeat for multiple part products.

Applicant - AKORN
The firm name holding legal responsibility for Triamcinolone Diacetate. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 085122
The FDA assigned number to Triamcinolone Diacetate. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Triamcinolone Diacetate. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code -
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Approved Prior to Jan 1, 1982
The date Triamcinolone Diacetate 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) - No
The pioneer or innovator of Triamcinolone Diacetate. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.

Type - DISCN
The group or category of approved drugs Triamcinolone Diacetate is in. Format is RX, OTC, DISCN.

Applicant Full Name - Akorn Inc
The full name of the firm holding legal responsibility for the new application of Triamcinolone Diacetate.

Triamcinolone Diacetate