Laryngotracheal Anesthesia Kit

   
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Laryngotracheal Anesthesia Kit


Drug - Laryngotracheal Anesthesia Kit
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) - Lidocaine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 4%
The potency of the active ingredient(s), Lidocaine Hydrochloride. May repeat for multiple part products.

Applicant - KENDALL IL
The firm name holding legal responsibility for Laryngotracheal Anesthesia Kit. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 087931
The FDA assigned number to Laryngotracheal Anesthesia Kit. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Laryngotracheal Anesthesia Kit. 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 - Jun 10, 1983
The date Laryngotracheal Anesthesia Kit 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 Laryngotracheal Anesthesia Kit. 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 Laryngotracheal Anesthesia Kit is in. Format is RX, OTC, DISCN.

Applicant Full Name - Kendall Co
The full name of the firm holding legal responsibility for the new application of Laryngotracheal Anesthesia Kit.

Laryngotracheal Anesthesia Kit