Optiray 240

   
Google
 
Web NewDrugInformation.com

Optiray 240


Drug - Optiray 240
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) - Ioversol
Multiple ingredients are in alphabetical order.

Strength - 51%
The potency of the active ingredient(s), Ioversol. May repeat for multiple part products.

Applicant - MALLINCKRODT
The firm name holding legal responsibility for Optiray 240. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 019710
The FDA assigned number to Optiray 240. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Optiray 240. 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 - Dec 30, 1988
The date Optiray 240 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 Optiray 240. 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 Optiray 240 is in. Format is RX, OTC, DISCN.

Applicant Full Name - Mallinckrodt Medical Inc
The full name of the firm holding legal responsibility for the new application of Optiray 240.

Optiray 240