Tolmetin Sodium

   
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Tolmetin Sodium


Drug - Tolmetin Sodium
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) - Tolmetin Sodium
Multiple ingredients are in alphabetical order.

Strength - EQ 200MG BASE
The potency of the active ingredient(s), Tolmetin Sodium. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 073588
The FDA assigned number to Tolmetin Sodium. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Tolmetin Sodium. 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 - Jul 31, 1992
The date Tolmetin Sodium 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 Tolmetin Sodium. 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 Tolmetin Sodium 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 Tolmetin Sodium.

Tolmetin Sodium