Celexa

   
Google
 
Web NewDrugInformation.com

Celexa


Drug - Celexa
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) - Citalopram Hydrobromide
Multiple ingredients are in alphabetical order.

Strength - EQ 60MG BASE
The potency of the active ingredient(s), Citalopram Hydrobromide. May repeat for multiple part products.

Applicant - FOREST LABS
The firm name holding legal responsibility for Celexa. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 020822
The FDA assigned number to Celexa. Format is nnnnnn.

Product Number - 004
The FDA assigned number to identify Celexa. 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 - Jul 17, 1998
The date Celexa 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 Celexa. 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 Celexa is in. Format is RX, OTC, DISCN.

Applicant Full Name - Forest Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Celexa.

Celexa