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  5. NDC Package Code: 66336-233-30 Arthritis Pain Reliever

NDC Package 66336-233-30 Arthritis Pain Reliever

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:
66336-233-30
Package Description:
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Code:
66336-233
Proprietary Name:
Arthritis Pain Reliever
Usage Information:
Do not take more than directed (see overdose warning)adultstake 2 caplets every 8 hours with water swallow whole - do not crush, chew, split or dissolve do not take more than 6 caplets in 24 hours do not use for more than 10 days unless directed by a doctorunder 18 years of ageask a doctor
11-Digit NDC Billing Format:
66336023330
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
    • Labeler Name:
    Dispensing Solutions, Inc.
    Sample Package:
    No
    Start Marketing Date:
    04-30-2002
    Listing Expiration Date:
    12-31-2017
    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
    66336-233-00100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 66336-233-30?

    The NDC Packaged Code 66336-233-30 is assigned to a package of 30 tablet, film coated, extended release in 1 bottle of Arthritis Pain Reliever, labeled by Dispensing Solutions, Inc.. The product's dosage form is and is administered via form.

    Is NDC 66336-233 included in the NDC Directory?

    No, Arthritis Pain Reliever with product code 66336-233 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Dispensing Solutions, Inc. on April 30, 2002 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 66336-233-30?

    The 11-digit format is 66336023330. 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
    5-3-266336-233-305-4-266336-0233-30