Cubicin

   
Google
 
Web NewDrugInformation.com

Cubicin


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

Dosage - INJECTABLE; IV (INFUSION)
The product dosage form and route separated by a semi-colon.

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

Strength - 500MG/VIAL
The potency of the active ingredient(s), Daptomycin. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 021572
The FDA assigned number to Cubicin. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Cubicin. 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 - Sep 12, 2003
The date Cubicin 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 Cubicin. 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 Cubicin is in. Format is RX, OTC, DISCN.

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

Cubicin