Uroplus Ds

   
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Uroplus Ds


Drug - Uroplus Ds
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 - SHIONOGI
The firm name holding legal responsibility for Uroplus Ds. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 071816
The FDA assigned number to Uroplus Ds. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Uroplus Ds. 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 - Sep 28, 1987
The date Uroplus Ds 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 Uroplus Ds. 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 Uroplus Ds is in. Format is RX, OTC, DISCN.

Applicant Full Name - Shionogi Usa Inc
The full name of the firm holding legal responsibility for the new application of Uroplus Ds.

Uroplus Ds