Kerlone

   
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Kerlone


Drug - Kerlone
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) - Betaxolol Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 10MG
The potency of the active ingredient(s), Betaxolol Hydrochloride. May repeat for multiple part products.

Applicant - LOREX
The firm name holding legal responsibility for Kerlone. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 019507
The FDA assigned number to Kerlone. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Kerlone. 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 - Oct 27, 1989
The date Kerlone 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 Kerlone. 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 Kerlone is in. Format is RX, OTC, DISCN.

Applicant Full Name - Lorex Pharmaceuticals
The full name of the firm holding legal responsibility for the new application of Kerlone.

Kerlone