Fosinopril Sodium And Hydrochlorothiazide

   
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Fosinopril Sodium And Hydrochlorothiazide


Drug - Fosinopril Sodium 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) - Fosinopril Sodium; Hydrochlorothiazide
Multiple ingredients are in alphabetical order.

Strength - 20MG;12.5MG
The potency of the active ingredient(s), Fosinopril Sodium; Hydrochlorothiazide. May repeat for multiple part products.

Applicant - WATSON LABS
The firm name holding legal responsibility for Fosinopril Sodium And Hydrochlorothiazide. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 077144
The FDA assigned number to Fosinopril Sodium And Hydrochlorothiazide. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Fosinopril Sodium 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 - Aug 16, 2005
The date Fosinopril Sodium 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 Fosinopril Sodium 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 Fosinopril Sodium And Hydrochlorothiazide is in. Format is RX, OTC, DISCN.

Applicant Full Name - Watson Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Fosinopril Sodium And Hydrochlorothiazide.

Fosinopril Sodium And Hydrochlorothiazide