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  5. NDC Package Code: 69729-782-10 Acetaminophen, Guaifenesin, Dextromethorphan Hbr, Phenylephrine Hcl

NDC Package 69729-782-10 Acetaminophen, Guaifenesin, Dextromethorphan Hbr, Phenylephrine Hcl

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:
69729-782-10
Package Description:
10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code:
69729-782
Proprietary Name:
Acetaminophen, Guaifenesin, Dextromethorphan Hbr, Phenylephrine Hcl
Usage Information:
Temporarily relieves common cold/flu symptoms:Nasal congestionSinus congestion & pressureCough due to minor throat & bronchial irritationMinor aches & painHeadacheFeverSore throatReduces swelling of nasal passagesTemporarily restore freer breathing through the nosePromotes nasal and/or sinus drainageHelps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive.
11-Digit NDC Billing Format:
69729078210
NDC to RxNorm Crosswalk:
  • RxCUI: 1656815 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1656815 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1656815 - APAP 325 MG / Dextromethorphan Hydrobromide 10 MG / Guaifenesin 200 MG / Phenylephrine Hydrochloride 5 MG Oral Capsule
    • Labeler Name:
    Opmx Llc
    Sample Package:
    No
    Start Marketing Date:
    02-18-2019
    Listing Expiration Date:
    12-31-2023
    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 69729-782-10?

    The NDC Packaged Code 69729-782-10 is assigned to a package of 10 capsule, liquid filled in 1 blister pack of Acetaminophen, Guaifenesin, Dextromethorphan Hbr, Phenylephrine Hcl, labeled by Opmx Llc. The product's dosage form is and is administered via form.

    Is NDC 69729-782 included in the NDC Directory?

    No, Acetaminophen, Guaifenesin, Dextromethorphan Hbr, Phenylephrine Hcl with product code 69729-782 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Opmx Llc on February 18, 2019 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 69729-782-10?

    The 11-digit format is 69729078210. 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
    5-3-269729-782-105-4-269729-0782-10