Thyrel Trh

   
Google
 
Web NewDrugInformation.com

Thyrel Trh


Drug - Thyrel Trh
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) - Protirelin
Multiple ingredients are in alphabetical order.

Strength - 0.5MG/ML
The potency of the active ingredient(s), Protirelin. May repeat for multiple part products.

Applicant - FERRING
The firm name holding legal responsibility for Thyrel Trh. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 018087
The FDA assigned number to Thyrel Trh. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Thyrel Trh. 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 Thyrel Trh 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 Thyrel Trh. 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 Thyrel Trh is in. Format is RX, OTC, DISCN.

Applicant Full Name - Ferring Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Thyrel Trh.

Thyrel Trh