Benazepril Hcl

   
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Benazepril Hcl


Drug - Benazepril 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) - Benazepril Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 40MG
The potency of the active ingredient(s), Benazepril Hydrochloride. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 076267
The FDA assigned number to Benazepril Hcl. Format is nnnnnn.

Product Number - 004
The FDA assigned number to identify Benazepril 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 - Feb 11, 2004
The date Benazepril 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 Benazepril 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 Benazepril Hcl is in. Format is RX, OTC, DISCN.

Applicant Full Name - Andrx Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Benazepril Hcl.

Benazepril Hcl