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  5. NDC Package Code: 52389-172-04 Nauzene

NDC Package 52389-172-04 Nauzene

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:
52389-172-04
Package Description:
118 mL in 1 BOTTLE, PLASTIC
Product Code:
52389-172
Proprietary Name:
Nauzene
Usage Information:
Read all package directions and warnings before use and use only as directed.Adults:  1 - 2 tablespoons (15 - 30 mL).Children:  Consult a doctor for appropriate dosage.Dosage may be repeated after 30 minutes not to exceed 6 doses in a 24-hour period unless advised by a doctor.For maximum effectiveness never dilute Nauzene or drink fluids of any kind immediately before or after taking Nauzene.Nauzene Liquid is intended for use by normally healthy persons only.Persons under 18 years of age should use only as directed by a doctor.
11-Digit NDC Billing Format:
52389017204
NDC to RxNorm Crosswalk:
  • RxCUI: 895045 - glucose 4.35 GM / fructose 4.17 GM / sodium citrate 0.921 GM in 15 mL Oral Solution
  • RxCUI: 895045 - fructose 278 MG/ML / glucose 290 MG/ML / sodium citrate 61.4 MG/ML Oral Solution
  • RxCUI: 895045 - fructose 4.17 GM / glucose 4.35 GM / sodium citrate 0.921 GM per 15 ML Oral Solution
    • Labeler Name:
    Alva-amco Pharmacal Companies, Inc.
    Sample Package:
    No
    Start Marketing Date:
    02-15-2000
    Listing Expiration Date:
    12-31-2018
    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 52389-172-04?

    The NDC Packaged Code 52389-172-04 is assigned to a package of 118 ml in 1 bottle, plastic of Nauzene, labeled by Alva-amco Pharmacal Companies, Inc.. The product's dosage form is and is administered via form.

    Is NDC 52389-172 included in the NDC Directory?

    No, Nauzene with product code 52389-172 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Alva-amco Pharmacal Companies, Inc. on February 15, 2000 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 52389-172-04?

    The 11-digit format is 52389017204. 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
    5-3-252389-172-045-4-252389-0172-04