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  5. NDC Package Code: 23359-023-16 Rydex

NDC Package 23359-023-16 Rydex

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
23359-023-16
Package Description:
473 mL in 1 BOTTLE
Product Code:
23359-023
Proprietary Name:
Rydex
Usage Information:
Do not exceed recommended dosage.Adults and children 12 years of ageand over:3 teaspoonfuls (15 mL) every 4 to 6 hours, not to exceed 18 teaspoonfuls in a 24 hour period.Children 6 to under 12 years of age:1 1/2 teaspoonfuls (7.5 mL) every 4 to 6 hours, not to exceed 9 teaspoonfuls in a 24 hour period.Not recommended for children under 6 years of age.
11-Digit NDC Billing Format:
23359002316
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
473 ML
NDC to RxNorm Crosswalk:
  • RxCUI: 994289 - codeine phosphate 6.33 MG / brompheniramine maleate 1.33 MG / pseudoephedrine HCl 10 MG in 5 mL Oral Solution
  • RxCUI: 994289 - brompheniramine maleate 0.27 MG/ML / codeine phosphate 1.27 MG/ML / pseudoephedrine hydrochloride 2 MG/ML Oral Solution
  • RxCUI: 994289 - brompheniramine maleate 1.33 MG / codeine phosphate 6.33 MG / pseudoephedrine hydrochloride 10 MG per 5 ML Oral Solution
Labeler Name:
Centurion Labs
Sample Package:
No
FDA Application Number:
part341
Marketing Category:
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date:
05-14-2010
Listing Expiration Date:
12-31-2017
Exclude Flag:
I
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.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 23359-023-16?

The NDC Packaged Code 23359-023-16 is assigned to a package of 473 ml in 1 bottle of Rydex, labeled by Centurion Labs. The product's dosage form is and is administered via form.This product is billed per "ML" milliliter and contains an estimated amount of 473 billable units per package.

Is NDC 23359-023 included in the NDC Directory?

No, Rydex with product code 23359-023 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Centurion Labs on May 14, 2010 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 23359-023-16?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 473.

What is the 11-digit format for NDC 23359-023-16?

The 11-digit format is 23359002316. 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
5-3-223359-023-165-4-223359-0023-16