Enalapril Maleate And Hydrochlorothiazide

   
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Enalapril Maleate And Hydrochlorothiazide


Drug - Enalapril Maleate And Hydrochlorothiazide
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) - Enalapril Maleate; Hydrochlorothiazide
Multiple ingredients are in alphabetical order.

Strength - 10MG;25MG
The potency of the active ingredient(s), Enalapril Maleate; Hydrochlorothiazide. May repeat for multiple part products.

Applicant - MYLAN
The firm name holding legal responsibility for Enalapril Maleate And Hydrochlorothiazide. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 075624
The FDA assigned number to Enalapril Maleate And Hydrochlorothiazide. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Enalapril Maleate And Hydrochlorothiazide. 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 - Sep 18, 2001
The date Enalapril Maleate And Hydrochlorothiazide 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 Enalapril Maleate And Hydrochlorothiazide. 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 Enalapril Maleate And Hydrochlorothiazide 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 Enalapril Maleate And Hydrochlorothiazide.

Enalapril Maleate And Hydrochlorothiazide