Amiloride Hcl And Hydrochlorothiazide


Amiloride Hcl And Hydrochlorothiazide

Drug - Amiloride Hcl And Hydrochlorothiazide
The trade name of the product as shown on the labeling.

The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Amiloride Hydrochloride; Hydrochlorothiazide
Multiple ingredients are in alphabetical order.

Strength - EQ 5MG ANHYDROUS;50MG
The potency of the active ingredient(s), Amiloride Hydrochloride; Hydrochlorothiazide. May repeat for multiple part products.

Applicant - TEVA
The firm name holding legal responsibility for Amiloride Hcl And Hydrochlorothiazide. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 070795
The FDA assigned number to Amiloride Hcl And Hydrochlorothiazide. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Amiloride Hcl 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 - Apr 17, 1988
The date Amiloride Hcl 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 Amiloride Hcl 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 Amiloride Hcl And Hydrochlorothiazide is in. Format is RX, OTC, DISCN.

Applicant Full Name - Teva Pharmaceuticals Usa Inc
The full name of the firm holding legal responsibility for the new application of Amiloride Hcl And Hydrochlorothiazide.

Amiloride Hcl And Hydrochlorothiazide