Celebrex

   
Google
 
Web NewDrugInformation.com

Celebrex


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

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

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

Strength - 200MG
The potency of the active ingredient(s), Celecoxib. May repeat for multiple part products.

Applicant - GD SEARLE LLC
The firm name holding legal responsibility for Celebrex. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 020998
The FDA assigned number to Celebrex. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Celebrex. 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 31, 1998
The date Celebrex 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 Celebrex. 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 Celebrex is in. Format is RX, OTC, DISCN.

Applicant Full Name - Gd Searle Llc
The full name of the firm holding legal responsibility for the new application of Celebrex.

Celebrex