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  5. NDC Package Code: 17856-0235-1 Hydrocodone Polistirex And Chlorpheniramine Polisitrex

NDC Package 17856-0235-1 Hydrocodone Polistirex And Chlorpheniramine Polisitrex

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:
17856-0235-1
Package Description:
5 mL in 1 CUP, UNIT-DOSE
Product Code:
17856-0235
Proprietary Name:
Hydrocodone Polistirex And Chlorpheniramine Polisitrex
Usage Information:
Hydrocodone polistirex and chlorpheniramine polistirex extended-release oral suspension is indicated for relief of cough and upper respiratory symptoms associated with allergy or a cold in adults and children 6 years of age and older.
11-Digit NDC Billing Format:
17856023501
NDC to RxNorm Crosswalk:
  • RxCUI: 1087459 - HYDROcodone polistirex 10 MG / chlorpheniramine polistirex 8 MG in 5 mL 12HR Extended Release Oral Suspension
  • RxCUI: 1087459 - 12 HR chlorpheniramine polistirex 1.6 MG/ML / hydrocodone polistirex 2 MG/ML Extended Release Suspension
  • RxCUI: 1087459 - hydrocodone polistirex 10 MG / chlorpheniramine polistirex 8 MG per 5 ML 12HR Extended Release Oral Suspension
    • Labeler Name:
    Atlantic Biologicals Corps
    Sample Package:
    No
    Start Marketing Date:
    08-16-2012
    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 17856-0235-1?

    The NDC Packaged Code 17856-0235-1 is assigned to a package of 5 ml in 1 cup, unit-dose of Hydrocodone Polistirex And Chlorpheniramine Polisitrex, labeled by Atlantic Biologicals Corps. The product's dosage form is and is administered via form.

    Is NDC 17856-0235 included in the NDC Directory?

    No, Hydrocodone Polistirex And Chlorpheniramine Polisitrex with product code 17856-0235 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Atlantic Biologicals Corps on August 16, 2012 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 17856-0235-1?

    The 11-digit format is 17856023501. 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
    5-4-117856-0235-15-4-217856-0235-01