Quinapril Hcl

   
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Quinapril Hcl


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

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

Applicant - AMIDE PHARM
The firm name holding legal responsibility for Quinapril Hcl. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 076459
The FDA assigned number to Quinapril Hcl. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Quinapril 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 - Dec 22, 2004
The date Quinapril 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 Quinapril 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 Quinapril Hcl is in. Format is RX, OTC, DISCN.

Applicant Full Name - Amide Pharmaceutical Inc
The full name of the firm holding legal responsibility for the new application of Quinapril Hcl.

Quinapril Hcl