NDC Package 55315-531-57 Extra Strength Pain Reliever

View Billable Units, 11-Digit Format, RxNorm

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:
55315-531-57
Package Description:
1 BOTTLE in 1 CARTON / 125 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Extra Strength Pain Reliever
Usage Information:
Do not take more than directed (see overdose warning)adults and children 12 years and overtake 2 tablets every 4 to 6 hours while symptoms lastdo not take more than 8 tablets in 24 hoursdo not take for more than 10 days unless directed by a doctorchildren under 12 years: do not use this product in children under 12 years of age; this will provide more than the recommended dose (overdose) of acetaminophen and may cause liver damage 
11-Digit NDC Billing Format:
55315053157
NDC to RxNorm Crosswalk:
  • RxCUI: 198440 - acetaminophen 500 MG Oral Tablet
  • RxCUI: 198440 - APAP 500 MG Oral Tablet
  • Labeler Name:
    Fred's, Inc.
    Sample Package:
    No
    Start Marketing Date:
    12-11-2005
    Listing Expiration Date:
    12-31-2019
    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
    55315-531-121 BOTTLE in 1 CARTON / 100 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 55315-531-57?

    The NDC Packaged Code 55315-531-57 is assigned to a package of 1 bottle in 1 carton / 125 tablet in 1 bottle of Extra Strength Pain Reliever, labeled by Fred's, Inc.. The product's dosage form is and is administered via form.

    Is NDC 55315-531 included in the NDC Directory?

    No, Extra Strength Pain Reliever with product code 55315-531 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Fred's, Inc. on December 11, 2005 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 55315-531-57?

    The 11-digit format is 55315053157. 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
    5-3-255315-531-575-4-255315-0531-57