Potassium Chloride In Dextrose And Sodium Chloride Injection
NDC Package 0264-7635-00
Package Information
Potassium Chloride In Dextrose And Sodium Chloride (dextrose, sodium chloride, and potassium chloride) injection is these intravenous solutions are indicated for use in adults and pediatric patients as sources of electrolytes, calories and water for hydration. This formulation utilizes a injection delivery system. Marketed by B. Braun Medical Inc., this product is identified by NDC 0264-7635 and is authorized under FDA application NDA019630.
Identification & Billing
- RxCUI: 1863605 - potassium chloride 20 MEQ / dextrose 5 % / sodium chloride 0.45 % in 1000 ML Injection
- RxCUI: 1863605 - 1000 ML glucose 50 MG/ML / potassium chloride 0.02 MEQ/ML / sodium chloride 4.5 MG/ML Injection
- RxCUI: 1863605 - 1000 ML Glucose 50 MG/ML / K+ Chloride 0.02 MEQ/ML / NaCl 4.5 MG/ML Injection
- RxCUI: 1863605 - 1000 ML Glucose 50 MG/ML / Pot Chloride 0.02 MEQ/ML / NaCl 4.5 MG/ML Injection
- RxCUI: 1863605 - potassium chloride 20 MEQ / dextrose 5 % / sodium chloride 0.45 % per 1000 ML Injection
Clinical Specifications
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Potassium Compounds - [CS]
- Potassium Salt - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 0264 - B. Braun Medical Inc.
- 0264-7635 - Potassium Chloride In Dextrose And Sodium Chloride
- 0264-7635-00 - 12 CONTAINER in 1 CASE / 1000 mL in 1 CONTAINER
- 0264-7635 - Potassium Chloride In Dextrose And Sodium Chloride
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 0264-7635-00 identifies a specific commercial package of 12 container in 1 case / 1000 ml in 1 container of Potassium Chloride In Dextrose And Sodium Chloride, a human prescription drug labeled by B. Braun Medical Inc.. This injection is formulated for intravenous use and contains dextrose, unspecified form; potassium chloride; sodium chloride as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by B. Braun Medical Inc. on February 17, 1988. The current certification is valid through December 31, 2026.
How is this B. Braun Medical Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00264763500. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.
