Tenuate

   
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Tenuate


Drug - Tenuate
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) - Diethylpropion Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 25MG
The potency of the active ingredient(s), Diethylpropion Hydrochloride. May repeat for multiple part products.

Applicant - AVENTIS PHARMS
The firm name holding legal responsibility for Tenuate. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 011722
The FDA assigned number to Tenuate. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Tenuate. 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 - Approved Prior to Jan 1, 1982
The date Tenuate 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) - Yes
The pioneer or innovator of Tenuate. 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 Tenuate is in. Format is RX, OTC, DISCN.

Applicant Full Name - Aventis Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Tenuate.

Tenuate