Acetazolamide Sodium

   
Google
 
Web NewDrugInformation.com

Acetazolamide Sodium


Drug - Acetazolamide Sodium
The trade name of the product as shown on the labeling.

Dosage - INJECTABLE; INJECTION
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Acetazolamide Sodium
Multiple ingredients are in alphabetical order.

Strength - EQ 500MG BASE/VIAL
The potency of the active ingredient(s), Acetazolamide Sodium. May repeat for multiple part products.

Applicant - HOSPIRA
The firm name holding legal responsibility for Acetazolamide Sodium. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 040108
The FDA assigned number to Acetazolamide Sodium. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Acetazolamide Sodium. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code - AP
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Oct 30, 1995
The date Acetazolamide Sodium 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 Acetazolamide Sodium. 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 Acetazolamide Sodium is in. Format is RX, OTC, DISCN.

Applicant Full Name - Hospira Inc
The full name of the firm holding legal responsibility for the new application of Acetazolamide Sodium.

Acetazolamide Sodium