Perphenazine And Amitriptyline Hcl

   
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Perphenazine And Amitriptyline Hcl


Drug - Perphenazine And Amitriptyline Hcl
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) - Amitriptyline Hydrochloride; Perphenazine
Multiple ingredients are in alphabetical order.

Strength - 25MG;4MG
The potency of the active ingredient(s), Amitriptyline Hydrochloride; Perphenazine. May repeat for multiple part products.

Applicant - MYLAN
The firm name holding legal responsibility for Perphenazine And Amitriptyline Hcl. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 070338
The FDA assigned number to Perphenazine And Amitriptyline Hcl. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Perphenazine And Amitriptyline Hcl. 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 - Nov 10, 1988
The date Perphenazine And Amitriptyline Hcl 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 Perphenazine And Amitriptyline Hcl. 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 Perphenazine And Amitriptyline Hcl is in. Format is RX, OTC, DISCN.

Applicant Full Name - Mylan Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Perphenazine And Amitriptyline Hcl.

Perphenazine And Amitriptyline Hcl