Sulfamethoxazole And Trimethoprim

   
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Sulfamethoxazole And Trimethoprim


Drug - Sulfamethoxazole And Trimethoprim
The trade name of the product as shown on the labeling.

Dosage - TABLET; ORAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Sulfamethoxazole; Trimethoprim
Multiple ingredients are in alphabetical order.

Strength - 800MG;160MG
The potency of the active ingredient(s), Sulfamethoxazole; Trimethoprim. May repeat for multiple part products.

Applicant - INTERPHARM
The firm name holding legal responsibility for Sulfamethoxazole And Trimethoprim. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 076899
The FDA assigned number to Sulfamethoxazole And Trimethoprim. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Sulfamethoxazole And Trimethoprim. 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 - Jan 27, 2005
The date Sulfamethoxazole And Trimethoprim 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 Sulfamethoxazole And Trimethoprim. 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 Sulfamethoxazole And Trimethoprim is in. Format is RX, OTC, DISCN.

Applicant Full Name - Interpharm Inc
The full name of the firm holding legal responsibility for the new application of Sulfamethoxazole And Trimethoprim.

Sulfamethoxazole And Trimethoprim