Potassium Chloride 0.037% In Dextrose 5% And Sodium Chloride 0.11% In Plastic Container

   
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Potassium Chloride 0.037% In Dextrose 5% And Sodium Chloride 0.11% In Plastic Container


Drug - Potassium Chloride 0.037% In Dextrose 5% And Sodium Chloride 0.11% 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) - Dextrose; Potassium Chloride; Sodium Chloride
Multiple ingredients are in alphabetical order.

Strength - 5GM/100ML;37MG/100ML;110MG/100ML
The potency of the active ingredient(s), Dextrose; Potassium Chloride; Sodium Chloride. May repeat for multiple part products.

Applicant - B BRAUN
The firm name holding legal responsibility for Potassium Chloride 0.037% In Dextrose 5% And Sodium Chloride 0.11% In Plastic Container. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 019630
The FDA assigned number to Potassium Chloride 0.037% In Dextrose 5% And Sodium Chloride 0.11% In Plastic Container. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Potassium Chloride 0.037% In Dextrose 5% And Sodium Chloride 0.11% 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 - Feb 17, 1988
The date Potassium Chloride 0.037% In Dextrose 5% And Sodium Chloride 0.11% 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 Potassium Chloride 0.037% In Dextrose 5% And Sodium Chloride 0.11% In Plastic Container. 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 Potassium Chloride 0.037% In Dextrose 5% And Sodium Chloride 0.11% 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 Potassium Chloride 0.037% In Dextrose 5% And Sodium Chloride 0.11% In Plastic Container.

Potassium Chloride 0.037% In Dextrose 5% And Sodium Chloride 0.11% In Plastic Container


Potassium Chloride 0.037% In Dextrose 5% And Sodium Chloride 0.11% In Plastic Container 5gm/100ml;37mg/100ml;110mg/100ml Injectable; Injection
Dextrose 5%, Sodium Chloride 0.45% And Potassium Chloride 0.22% In Plastic Container 5gm/100ml;220mg/100ml;450mg/100ml Injectable; Injection
Dextrose 5%, Sodium Chloride 0.45% And Potassium Chloride 0.3% In Plastic Container 5gm/100ml;300mg/100ml;450mg/100ml Injectable; Injection
Dextrose 5%, Sodium Chloride 0.45% And Potassium Chloride 15meq In Plastic Container 5gm/100ml;224mg/100ml;450mg/100ml Injectable; Injection
Dextrose 5%, Sodium Chloride 0.45% And Potassium Chloride 20meq (k) In Plastic Container 5gm/100ml;300mg/100ml;450mg/100ml Injectable; Injection
Dextrose 5%, Sodium Chloride 0.45% And Potassium Chloride 20meq (k) In Plastic Container 5gm/100ml;300mg/100ml;450mg/100ml Injectable; Injection
Dextrose 5%, Sodium Chloride 0.45% And Potassium Chloride 5meq In Plastic Container 5gm/100ml;75mg/100ml;450mg/100ml Injectable; Injection
Potassium Chloride 0.037% In Dextrose 10% And Sodium Chloride 0.2% In Plastic Container 10gm/100ml;37mg/100ml;200mg/100ml Injectable; Injection
Potassium Chloride 0.037% In Dextrose 10% And Sodium Chloride 0.45% In Plastic Container 10gm/100ml;37mg/100ml;450mg/100ml Injectable; Injection
Potassium Chloride 0.037% In Dextrose 10% And Sodium Chloride 0.9% In Plastic Container 10gm/100ml;37mg/100ml;900mg/100ml Injectable; Injection

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