Mexitil

   
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Mexitil


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

Dosage - CAPSULE; ORAL
The product dosage form and route separated by a semi-colon.

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

Strength - 200MG
The potency of the active ingredient(s), Mexiletine Hydrochloride. May repeat for multiple part products.

Applicant - BOEHRINGER INGELHEIM
The firm name holding legal responsibility for Mexitil. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 018873
The FDA assigned number to Mexitil. Format is nnnnnn.

Product Number - 003
The FDA assigned number to identify Mexitil. 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 - Dec 30, 1985
The date Mexitil 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 Mexitil. 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 Mexitil is in. Format is RX, OTC, DISCN.

Applicant Full Name - Boehringer Ingelheim
The full name of the firm holding legal responsibility for the new application of Mexitil.

Mexitil