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  5. NDC Package Code: 59726-669-10 Arthritispain Relief

NDC Package 59726-669-10 Arthritispain Relief

Acetaminophen Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

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:
59726-669-10
Package Description:
1 BOTTLE, PLASTIC in 1 BOX / 100 TABLET in 1 BOTTLE, PLASTIC
Product Code:
59726-669
Proprietary Name:
Arthritispain Relief
Non-Proprietary Name:
Acetaminophen
Substance Name:
Acetaminophen
Usage Information:
This drug is used to treat mild to moderate pain (from headaches, menstrual periods, toothaches, backaches, osteoarthritis, or cold/flu aches and pains) and to reduce fever.
11-Digit NDC Billing Format:
59726066910
NDC to RxNorm Crosswalk:
  • RxCUI: 1148399 - acetaminophen 650 MG 8HR Extended Release Oral Tablet
  • RxCUI: 1148399 - 8 HR acetaminophen 650 MG Extended Release Oral Tablet
  • RxCUI: 1148399 - 8 HR APAP 650 MG Extended Release Oral Tablet
  • RxCUI: 1148399 - acetaminophen 650 MG 8 HR Extended Release Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    P & L Development, Llc
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACETAMINOPHEN 650 mg/1
    • Sample Package:
    No
    FDA Application Number:
    ANDA207035
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-30-2021
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    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 59726-669-10?

    The NDC Packaged Code 59726-669-10 is assigned to a package of 1 bottle, plastic in 1 box / 100 tablet in 1 bottle, plastic of Arthritispain Relief, a human over the counter drug labeled by P & L Development, Llc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 59726-669 included in the NDC Directory?

    Yes, Arthritispain Relief with product code 59726-669 is active and included in the NDC Directory. The product was first marketed by P & L Development, Llc on April 30, 2021 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 59726-669-10?

    The 11-digit format is 59726066910. 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
    5-3-259726-669-105-4-259726-0669-10