Plenaxis

   
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Plenaxis


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

Dosage - INJECTABLE; INTRAMUSCULAR
The product dosage form and route separated by a semi-colon.

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

Strength - 100MG/VIAL
The potency of the active ingredient(s), Abarelix. May repeat for multiple part products.

Applicant - PRAECIS
The firm name holding legal responsibility for Plenaxis. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 021320
The FDA assigned number to Plenaxis. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Plenaxis. 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 - Nov 25, 2003
The date Plenaxis 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 Plenaxis. 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 Plenaxis is in. Format is RX, OTC, DISCN.

Applicant Full Name - Praecis Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Plenaxis.

Plenaxis