Effexor Xr

   
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Effexor Xr


Drug - Effexor Xr
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) - Venlafaxine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - EQ 150MG BASE
The potency of the active ingredient(s), Venlafaxine Hydrochloride. May repeat for multiple part products.

Applicant - WYETH PHARMS INC
The firm name holding legal responsibility for Effexor Xr. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 020699
The FDA assigned number to Effexor Xr. Format is nnnnnn.

Product Number - 004
The FDA assigned number to identify Effexor Xr. 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 20, 1997
The date Effexor Xr 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 Effexor Xr. 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 Effexor Xr is in. Format is RX, OTC, DISCN.

Applicant Full Name - Wyeth Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Effexor Xr.

Effexor Xr