Aricept Odt

   
Google
 
Web NewDrugInformation.com

Aricept Odt


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

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

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

Strength - 10MG
The potency of the active ingredient(s), Donepezil Hydrochloride. May repeat for multiple part products.

Applicant - EISAI MEDCL RES
The firm name holding legal responsibility for Aricept Odt. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 021720
The FDA assigned number to Aricept Odt. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Aricept Odt. 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 - Oct 18, 2004
The date Aricept Odt 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) - Yes
The pioneer or innovator of Aricept Odt. 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 Aricept Odt is in. Format is RX, OTC, DISCN.

Applicant Full Name - Eisai Medical Research Inc
The full name of the firm holding legal responsibility for the new application of Aricept Odt.

Aricept Odt