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  5. NDC Package Code: 58605-101-20 Maxifed

NDC Package 58605-101-20 Maxifed

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:
58605-101-20
Package Description:
20 TABLET in 1 BLISTER PACK
Product Code:
58605-101
Proprietary Name:
Maxifed
Usage Information:
Do not exceed recommended dosage.Adults and children 12 years of age and over:1 tablet by mouth every 4 hours, not to exceed 4 tablets in 24 hours, or as directed by a doctor.Children 6 to under 12 years of age:½ tablet by mouth every 4 hours, not to exceed 2 tablets in 24 hours, or as directed by a doctor.Children 2 to under 6 years of ageconsult a doctor
11-Digit NDC Billing Format:
58605010120
NDC to RxNorm Crosswalk:
  • RxCUI: 2003123 - guaiFENesin 360 MG / pseudoephedrine HCl 60 MG Oral Tablet
  • RxCUI: 2003123 - guaifenesin 360 MG / pseudoephedrine hydrochloride 60 MG Oral Tablet
    • Labeler Name:
    Mcr American Pharmaceuticals, Inc.
    Sample Package:
    Yes
    Start Marketing Date:
    04-01-2018
    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
    58605-101-01100 TABLET in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 58605-101-20?

    The NDC Packaged Code 58605-101-20 is assigned to a package of 20 tablet in 1 blister pack of Maxifed, labeled by Mcr American Pharmaceuticals, Inc.. The product's dosage form is and is administered via form.

    Is NDC 58605-101 included in the NDC Directory?

    No, Maxifed with product code 58605-101 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Mcr American Pharmaceuticals, Inc. on April 01, 2018 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 11-digit format for NDC 58605-101-20?

    The 11-digit format is 58605010120. 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
    5-3-258605-101-205-4-258605-0101-20