NDC Package 17271-735-06 Dextrose And Sodium Chloride

Dextrose Monohydrate And Sodium Chloride Injection, Solution Intravenous - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
17271-735-06
Package Description:
20 BAG in 1 CASE / 500 mL in 1 BAG
Product Code:
Proprietary Name:
Dextrose And Sodium Chloride
Non-Proprietary Name:
Dextrose Monohydrate And Sodium Chloride
Substance Name:
Dextrose Monohydrate; Sodium Chloride
Usage Information:
Intravenous solutions containing dextrose and sodium chloride are indicated for parenteral replenishment of fluid, minimal carbohydrate calories, and sodium chloride as required by the clinical condition of the patient.
11-Digit NDC Billing Format:
17271073506
NDC to RxNorm Crosswalk:
  • RxCUI: 1795344 - dextrose 5 % / sodium chloride 0.9 % in 500 ML Injection
  • RxCUI: 1795344 - 500 ML glucose 50 MG/ML / sodium chloride 9 MG/ML Injection
  • RxCUI: 1795344 - 500 ML Glucose 50 MG/ML / NaCl 9 MG/ML Injection
  • RxCUI: 1795344 - dextrose 5 % / sodium chloride 0.9 % per 500 ML Injection
  • RxCUI: 1795346 - dextrose 5 % / sodium chloride 0.9 % in 1000 ML Injection
Product Type:
Human Prescription Drug
Labeler Name:
Becton Dickinson And Company
Dosage Form:
Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
Administration Route(s):
Intravenous - Administration within or into a vein or veins.
Sample Package:
No
FDA Application Number:
ANDA211211
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
10-26-2020
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

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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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
17271-735-0710 BAG in 1 CASE / 1000 mL in 1 BAG

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 17271-735-06?

The NDC Packaged Code 17271-735-06 is assigned to a package of 20 bag in 1 case / 500 ml in 1 bag of Dextrose And Sodium Chloride, a human prescription drug labeled by Becton Dickinson And Company. The product's dosage form is injection, solution and is administered via intravenous form.

Is NDC 17271-735 included in the NDC Directory?

Yes, Dextrose And Sodium Chloride with product code 17271-735 is active and included in the NDC Directory. The product was first marketed by Becton Dickinson And Company on October 26, 2020 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 17271-735-06?

The 11-digit format is 17271073506. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-217271-735-065-4-217271-0735-06