Copper T Model Tcu 380a

   
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Copper T Model Tcu 380a


Drug - Copper T Model Tcu 380a
The trade name of the product as shown on the labeling.

Dosage - INTRAUTERINE DEVICE; INTRAUTERINE
The product dosage form and route separated by a semi-colon.

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

Strength - 309MG/COPPER
The potency of the active ingredient(s), Copper. May repeat for multiple part products.

Applicant - FEI
The firm name holding legal responsibility for Copper T Model Tcu 380a. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 018680
The FDA assigned number to Copper T Model Tcu 380a. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Copper T Model Tcu 380a. 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 - Nov 15, 1984
The date Copper T Model Tcu 380a 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 Copper T Model Tcu 380a. 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 Copper T Model Tcu 380a is in. Format is RX, OTC, DISCN.

Applicant Full Name - Fei Womens Health Llc
The full name of the firm holding legal responsibility for the new application of Copper T Model Tcu 380a.

Copper T Model Tcu 380a