Euthroid-3

   
Google
 
Web NewDrugInformation.com

Euthroid-3


Drug - Euthroid-3
The trade name of the product as shown on the labeling.

Dosage - TABLET; ORAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Liotrix (t4;t3)
Multiple ingredients are in alphabetical order.

Strength - 0.18MG;0.045MG
The potency of the active ingredient(s), Liotrix (t4;t3). May repeat for multiple part products.

Applicant - PARKE DAVIS
The firm name holding legal responsibility for Euthroid-3. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 016680
The FDA assigned number to Euthroid-3. Format is nnnnnn.

Product Number - 004
The FDA assigned number to identify Euthroid-3. 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 Euthroid-3 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 Euthroid-3. 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 Euthroid-3 is in. Format is RX, OTC, DISCN.

Applicant Full Name - Parke Davis Div Warner Lambert Co
The full name of the firm holding legal responsibility for the new application of Euthroid-3.

Euthroid-3