Chlordiazepoxide And Amitriptyline Hcl

   
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Chlordiazepoxide And Amitriptyline Hcl


Drug - Chlordiazepoxide 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; Chlordiazepoxide
Multiple ingredients are in alphabetical order.

Strength - EQ 25MG BASE;10MG
The potency of the active ingredient(s), Amitriptyline Hydrochloride; Chlordiazepoxide. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 072278
The FDA assigned number to Chlordiazepoxide And Amitriptyline Hcl. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Chlordiazepoxide 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 - May 9, 1988
The date Chlordiazepoxide 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) - No
The pioneer or innovator of Chlordiazepoxide 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 Chlordiazepoxide And Amitriptyline Hcl is in. Format is RX, OTC, DISCN.

Applicant Full Name - Par Pharmaceutical Inc
The full name of the firm holding legal responsibility for the new application of Chlordiazepoxide And Amitriptyline Hcl.

Chlordiazepoxide And Amitriptyline Hcl