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  5. NDC Package Code: 11523-0523-1 Acetaminophen, Dextromethorpha Hydrobromide, Guaifenesin

NDC Package 11523-0523-1 Acetaminophen, Dextromethorpha Hydrobromide, Guaifenesin

Capsule, Liquid Filled - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
11523-0523-1
Package Description:
1 BAG in 1 CASE / 5000 CAPSULE, LIQUID FILLED in 1 BAG
Product Code:
11523-0523
Non-Proprietary Name:
Acetaminophen, Dextromethorpha Hydrobromide, Guaifenesin
Substance Name:
Acetaminophen; Dextromethorphan Hydrobromide; Guaifenesin
11-Digit NDC Billing Format:
11523052301
Product Type:
Drug For Further Processing
Labeler Name:
Bayer Healthcare Llc.
Dosage Form:
Capsule, Liquid Filled - A solid dosage form in which the drug is enclosed within a soluble, gelatin shell which is plasticized by the addition of a polyol, such as sorbitol or glycerin, and is therefore of a somewhat thicker consistency than that of a hard shell capsule; typically, the active ingredients are dissolved or suspended in a liquid vehicle.
Active Ingredient(s):
  • ACETAMINOPHEN 325 mg/1
  • DEXTROMETHORPHAN HYDROBROMIDE 10 mg/1
  • GUAIFENESIN 200 mg/1
    • Sample Package:
    N/A
    Marketing Category:
    DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
    Start Marketing Date:
    03-01-2020
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Unfinished Product:
    Yes
    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 11523-0523-1?

    The NDC Packaged Code 11523-0523-1 is assigned to an UNFINISHED drug package of 1 bag in 1 case / 5000 capsule, liquid filled in 1 bag of Acetaminophen, Dextromethorpha Hydrobromide, Guaifenesin, drug for further processing labeled by Bayer Healthcare Llc.. The product's dosage form is capsule, liquid filled and is administered via form.

    Is NDC 11523-0523 included in the NDC Directory?

    Yes, Acetaminophen, Dextromethorpha Hydrobromide, Guaifenesin is an UNFINISHED PRODUCT with code 11523-0523 that is active and included in the NDC Directory. The product was first marketed by Bayer Healthcare Llc. on March 01, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 11523-0523-1?

    The 11-digit format is 11523052301. 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
    5-4-111523-0523-15-4-211523-0523-01