Timolol Maleate

   
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Timolol Maleate


Drug - Timolol Maleate
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) - Timolol Maleate
Multiple ingredients are in alphabetical order.

Strength - 20MG
The potency of the active ingredient(s), Timolol Maleate. May repeat for multiple part products.

Applicant - SANDOZ
The firm name holding legal responsibility for Timolol Maleate. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 072552
The FDA assigned number to Timolol Maleate. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Timolol Maleate. 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 - Apr 13, 1989
The date Timolol Maleate 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 Timolol Maleate. 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 Timolol Maleate is in. Format is RX, OTC, DISCN.

Applicant Full Name - Sandoz Inc
The full name of the firm holding legal responsibility for the new application of Timolol Maleate.

Timolol Maleate