Inulin And Sodium Chloride

   
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Inulin And Sodium Chloride


Drug - Inulin And Sodium Chloride
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) - Inulin
Multiple ingredients are in alphabetical order.

Strength - 100MG/ML
The potency of the active ingredient(s), Inulin. May repeat for multiple part products.

Applicant - ISO TEX
The firm name holding legal responsibility for Inulin And Sodium Chloride. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 002282
The FDA assigned number to Inulin And Sodium Chloride. Format is nnnnnn.

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

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

Approval Date - Approved Prior to Jan 1, 1982
The date Inulin And Sodium Chloride 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 Inulin And Sodium Chloride. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.

Type - DISCN
The group or category of approved drugs Inulin And Sodium Chloride is in. Format is RX, OTC, DISCN.

Applicant Full Name - Iso Tex Diagnostics Inc
The full name of the firm holding legal responsibility for the new application of Inulin And Sodium Chloride.

Inulin And Sodium Chloride