Nystatin And Triamcinolone Acetonide

   
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Nystatin And Triamcinolone Acetonide


Drug - Nystatin And Triamcinolone Acetonide
The trade name of the product as shown on the labeling.

Dosage - CREAM; TOPICAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Nystatin; Triamcinolone Acetonide
Multiple ingredients are in alphabetical order.

Strength - 100,000 UNITS/GM;0.1%
The potency of the active ingredient(s), Nystatin; Triamcinolone Acetonide. May repeat for multiple part products.

Applicant - TARO
The firm name holding legal responsibility for Nystatin And Triamcinolone Acetonide. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 062364
The FDA assigned number to Nystatin And Triamcinolone Acetonide. Format is nnnnnn.

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

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

Approval Date - Dec 22, 1987
The date Nystatin And Triamcinolone Acetonide 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 Nystatin And Triamcinolone Acetonide. 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 Nystatin And Triamcinolone Acetonide is in. Format is RX, OTC, DISCN.

Applicant Full Name - Taro Pharmaceuticals Usa Inc
The full name of the firm holding legal responsibility for the new application of Nystatin And Triamcinolone Acetonide.

Nystatin And Triamcinolone Acetonide