Trimipramine Maleate

   
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Trimipramine Maleate


Drug - Trimipramine Maleate
The trade name of the product as shown on the labeling.

Dosage - CAPSULE; ORAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Trimipramine Maleate
Multiple ingredients are in alphabetical order.

Strength - EQ 100MG BASE
The potency of the active ingredient(s), Trimipramine Maleate. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 071285
The FDA assigned number to Trimipramine Maleate. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Trimipramine Maleate. 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 8, 1987
The date Trimipramine 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 Trimipramine Maleate. 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 Trimipramine Maleate is in. Format is RX, OTC, DISCN.

Applicant Full Name - Usl Pharma Inc
The full name of the firm holding legal responsibility for the new application of Trimipramine Maleate.

Trimipramine Maleate