Adriamycin Rdf

   
Google
 
Web NewDrugInformation.com

Adriamycin Rdf


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

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

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

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

Applicant - PHARMACIA AND UPJOHN
The firm name holding legal responsibility for Adriamycin Rdf. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 050467
The FDA assigned number to Adriamycin Rdf. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Adriamycin Rdf. 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 - Approved Prior to Jan 1, 1982
The date Adriamycin Rdf 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 Adriamycin Rdf. 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 Adriamycin Rdf is in. Format is RX, OTC, DISCN.

Applicant Full Name - Pharmacia And Upjohn Co
The full name of the firm holding legal responsibility for the new application of Adriamycin Rdf.

Adriamycin Rdf