Detrol La

   
Google
 
Web NewDrugInformation.com

Detrol La


Drug - Detrol La
The trade name of the product as shown on the labeling.

Dosage - CAPSULE, EXTENDED RELEASE; ORAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Tolterodine Tartrate
Multiple ingredients are in alphabetical order.

Strength - 2MG
The potency of the active ingredient(s), Tolterodine Tartrate. May repeat for multiple part products.

Applicant - PHARMACIA AND UPJOHN
The firm name holding legal responsibility for Detrol La. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 021228
The FDA assigned number to Detrol La. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Detrol La. 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 - Dec 22, 2000
The date Detrol La 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 Detrol La. 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 Detrol La is in. Format is RX, OTC, DISCN.

Applicant Full Name - Pharmacia And Upjohn Co
The full name of the firm holding legal responsibility for the new application of Detrol La.

Detrol La