Fluoroplex

   
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Fluoroplex


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

Dosage - SOLUTION; TOPICAL
The product dosage form and route separated by a semi-colon.

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

Strength - 1%
The potency of the active ingredient(s), Fluorouracil. May repeat for multiple part products.

Applicant - ALLERGAN HERBERT
The firm name holding legal responsibility for Fluoroplex. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 016765
The FDA assigned number to Fluoroplex. Format is nnnnnn.

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

Applicant Full Name - Allergan Herbert Div Allergan Inc
The full name of the firm holding legal responsibility for the new application of Fluoroplex.

Fluoroplex