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  5. NDC Package Code: 72162-1670-2 Guaifenesin And Dextromethorphan Hydrobromide

NDC Package 72162-1670-2 Guaifenesin And Dextromethorphan Hydrobromide

Syrup Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
72162-1670-2
Package Description:
237 mL in 1 BOTTLE, PLASTIC
Product Code:
72162-1670
Proprietary Name:
Guaifenesin And Dextromethorphan Hydrobromide
Non-Proprietary Name:
Guaifenesin And Dextromethorphan Hydrobromide
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin
Usage Information:
Do not take more than 6 doses in any 24-hour period. This adult product is not intended for use in children under 12 years of ageadults and children 12 years and over2 teaspoonfuls (TSP) every 4 hourschildren under 12 yearsDO NOT USE
11-Digit NDC Billing Format:
72162167002
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
237 ML
NDC to RxNorm Crosswalk:
  • RxCUI: 996520 - dextromethorphan HBr 20 MG / guaiFENesin 200 MG in 10 mL Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 10 MG / guaifenesin 100 MG per 5 ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 15 MG / guaifenesin 150 MG per 7.5 ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 20 MG / guaifenesin 200 MG per 10 ML Oral Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Bryant Ranch Prepack
    Dosage Form:
    Syrup - An oral solution containing high concentrations of sucrose or other sugars; the term has also been used to include any other liquid dosage form prepared in a sweet and viscid vehicle, including oral suspensions.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • DEXTROMETHORPHAN HYDROBROMIDE 10 mg/5mL
  • GUAIFENESIN 100 mg/5mL
    • Pharmacologic Class(es):
  • Decreased Respiratory Secretion Viscosity - [PE] (Physiologic Effect)
  • Expectorant - [EPC] (Established Pharmacologic Class)
  • Increased Respiratory Secretions - [PE] (Physiologic Effect)
  • Sigma-1 Agonist - [EPC] (Established Pharmacologic Class)
  • Sigma-1 Receptor Agonists - [MoA] (Mechanism of Action)
  • Uncompetitive N-methyl-D-aspartate Receptor Antagonist - [EPC] (Established Pharmacologic Class)
  • Uncompetitive NMDA Receptor Antagonists - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-14-2016
    Listing Expiration Date:
    12-31-2025
    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 72162-1670-2?

    The NDC Packaged Code 72162-1670-2 is assigned to a package of 237 ml in 1 bottle, plastic of Guaifenesin And Dextromethorphan Hydrobromide, a human over the counter drug labeled by Bryant Ranch Prepack. The product's dosage form is syrup and is administered via oral form.This product is billed per "ML" milliliter and contains an estimated amount of 237 billable units per package.

    Is NDC 72162-1670 included in the NDC Directory?

    Yes, Guaifenesin And Dextromethorphan Hydrobromide with product code 72162-1670 is active and included in the NDC Directory. The product was first marketed by Bryant Ranch Prepack on June 14, 2016 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 72162-1670-2?

    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 237.

    What is the 11-digit format for NDC 72162-1670-2?

    The 11-digit format is 72162167002. 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 5-4-1 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
    5-4-172162-1670-25-4-272162-1670-02