Tricor
Drug - Tricor
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) -
Fenofibrate
Multiple ingredients are in alphabetical order.
Strength -
160MG
The potency of the active ingredient(s), Fenofibrate. May repeat for multiple part products.
Applicant -
ABBOTT
The firm name holding legal responsibility for Tricor. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
021203
The FDA assigned number to Tricor. Format is nnnnnn.
Product Number -
003
The FDA assigned number to identify Tricor. Each strength is a separate product. May repeat for multiple part products. Format is nnn.
Therapeutic Equivalence (TE) Code -
AB
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.
Approval Date -
Sep 4, 2001
The date Tricor 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 Tricor. 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 Tricor is in. Format is RX, OTC, DISCN.
Applicant Full Name -
Abbott Laboratories
The full name of the firm holding legal responsibility for the new application of Tricor.
Tricor
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