Lidoderm

   
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Lidoderm


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

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

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

Strength - 5%
The potency of the active ingredient(s), Lidocaine. May repeat for multiple part products.

Applicant - TEIKOKU PHARMA USA
The firm name holding legal responsibility for Lidoderm. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 020612
The FDA assigned number to Lidoderm. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Lidoderm. 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 - Mar 19, 1999
The date Lidoderm 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 Lidoderm. 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 Lidoderm is in. Format is RX, OTC, DISCN.

Applicant Full Name - Teikoku Pharma Usa Inc
The full name of the firm holding legal responsibility for the new application of Lidoderm.

Lidoderm