Cartrol

   
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Cartrol


Drug - Cartrol
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) - Carteolol Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 2.5MG
The potency of the active ingredient(s), Carteolol Hydrochloride. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 019204
The FDA assigned number to Cartrol. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Cartrol. 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 - Dec 28, 1988
The date Cartrol 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 Cartrol. 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 Cartrol is in. Format is RX, OTC, DISCN.

Applicant Full Name - Abbott Laboratories
The full name of the firm holding legal responsibility for the new application of Cartrol.

Cartrol