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  5. NDC Package Code: 17856-0771-2 Docu Liquid

NDC Package 17856-0771-2 Docu Liquid

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
17856-0771-2
Package Description:
72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 10 mL in 1 CUP, UNIT-DOSE
Product Code:
17856-0771
Proprietary Name:
Docu Liquid
Usage Information:
•may be taken once daily or in divided doses•give dose in 1/2 glass of milk, fruit juice or infant formula to mask bitter taste and prevent throat irritationadults and children over 121 to 7 teaspoonschildren 2 to under 121 to 3 teaspoonschildren under 2ask a doctor
11-Digit NDC Billing Format:
17856077102
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1248119 - docusate sodium 50 MG in 5 mL Oral Suspension
  • RxCUI: 1248119 - docusate sodium 10 MG/ML Oral Suspension
  • RxCUI: 1248119 - docusate sodium 100 MG per 10 ML Oral Suspension
  • RxCUI: 1248119 - docusate sodium 150 MG per 15 ML Oral Suspension
  • RxCUI: 1248119 - docusate sodium 50 MG per 5 ML Oral Suspension
    • Labeler Name:
    Atlantic Biologicals Corp.
    Sample Package:
    No
    Start Marketing Date:
    08-01-1997
    Listing Expiration Date:
    12-31-2021
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    17856-0771-150 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 25 mL in 1 CUP, UNIT-DOSE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 17856-0771-2?

    The NDC Packaged Code 17856-0771-2 is assigned to a package of 72 cup, unit-dose in 1 box, unit-dose / 10 ml in 1 cup, unit-dose of Docu Liquid, labeled by Atlantic Biologicals Corp.. The product's dosage form is and is administered via form.

    Is NDC 17856-0771 included in the NDC Directory?

    No, Docu Liquid with product code 17856-0771 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Atlantic Biologicals Corp. on August 01, 1997 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 17856-0771-2?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 17856-0771-2?

    The 11-digit format is 17856077102. 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
    5-4-117856-0771-25-4-217856-0771-02