Sodium Chloride 0.9% And Potassium Chloride 0.3% In Plastic Container

   
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Sodium Chloride 0.9% And Potassium Chloride 0.3% In Plastic Container


Drug - Sodium Chloride 0.9% And Potassium Chloride 0.3% In Plastic Container
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) - Potassium Chloride; Sodium Chloride
Multiple ingredients are in alphabetical order.

Strength - 300MG/100ML;900MG/100ML
The potency of the active ingredient(s), Potassium Chloride; Sodium Chloride. May repeat for multiple part products.

Applicant - B BRAUN
The firm name holding legal responsibility for Sodium Chloride 0.9% And Potassium Chloride 0.3% In Plastic Container. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 018722
The FDA assigned number to Sodium Chloride 0.9% And Potassium Chloride 0.3% In Plastic Container. Format is nnnnnn.

Product Number - 004
The FDA assigned number to identify Sodium Chloride 0.9% And Potassium Chloride 0.3% In Plastic Container. 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 - Nov 9, 1982
The date Sodium Chloride 0.9% And Potassium Chloride 0.3% In Plastic Container 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 Sodium Chloride 0.9% And Potassium Chloride 0.3% In Plastic Container. 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 Sodium Chloride 0.9% And Potassium Chloride 0.3% In Plastic Container is in. Format is RX, OTC, DISCN.

Applicant Full Name - B Braun Medical Inc
The full name of the firm holding legal responsibility for the new application of Sodium Chloride 0.9% And Potassium Chloride 0.3% In Plastic Container.

Sodium Chloride 0.9% And Potassium Chloride 0.3% In Plastic Container


Potassium Chloride 20meq In Sodium Chloride 0.9% In Plastic Container 149mg/100ml;900mg/100ml Injectable; Injection
Potassium Chloride 40meq In Sodium Chloride 0.9% In Plastic Container 298mg/100ml;900mg/100ml Injectable; Injection
Sodium Chloride 0.9% And Potassium Chloride 0.075% In Plastic Container 75mg/100ml;900mg/100ml Injectable; Injection
Sodium Chloride 0.9% And Potassium Chloride 0.075% In Plastic Container 75mg/100ml;900mg/100ml Injectable; Injection
Sodium Chloride 0.9% And Potassium Chloride 0.15% In Plastic Container 150mg/100ml;900mg/100ml Injectable; Injection
Sodium Chloride 0.9% And Potassium Chloride 0.15% In Plastic Container 150mg/100ml;900mg/100ml Injectable; Injection
Sodium Chloride 0.9% And Potassium Chloride 0.22% In Plastic Container 220mg/100ml;900mg/100ml Injectable; Injection
Sodium Chloride 0.9% And Potassium Chloride 0.224% 224mg/100ml;900mg/100ml Injectable; Injection
Sodium Chloride 0.9% And Potassium Chloride 0.3% In Plastic Container 300mg/100ml;900mg/100ml Injectable; Injection
Potassium Chloride 0.3% In Sodium Chloride 0.9% In Plastic Container 300mg/100ml;900mg/100ml Injectable; Injection

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