Nystatin-triamcinolone Acetonide

   
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Nystatin-triamcinolone Acetonide


Drug - Nystatin-triamcinolone Acetonide
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) - 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 - FOUGERA
The firm name holding legal responsibility for Nystatin-triamcinolone Acetonide. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 062602
The FDA assigned number to Nystatin-triamcinolone Acetonide. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Nystatin-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 - Oct 9, 1985
The date Nystatin-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) - No
The pioneer or innovator of Nystatin-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-triamcinolone Acetonide is in. Format is RX, OTC, DISCN.

Applicant Full Name - E Fougera Div Altana Inc
The full name of the firm holding legal responsibility for the new application of Nystatin-triamcinolone Acetonide.

Nystatin-triamcinolone Acetonide