Enalapril Maleate

   
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Enalapril Maleate


Drug - Enalapril Maleate
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
Multiple ingredients are in alphabetical order.

Strength - 2.5MG
The potency of the active ingredient(s), Enalapril Maleate. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 075178
The FDA assigned number to Enalapril Maleate. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Enalapril Maleate. 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 - Mar 23, 2001
The date Enalapril Maleate 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. 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 is in. Format is RX, OTC, DISCN.

Applicant Full Name - Torpharm Inc
The full name of the firm holding legal responsibility for the new application of Enalapril Maleate.

Enalapril Maleate