Sunmark Arthritis Pain Reliever
NDC Package 49348-921-09

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
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.

Sunmark Arthritis Pain Reliever is 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. Marketed by Sunmark, this product is identified by NDC 49348-921 and is authorized under FDA application ANDA076200.

Identification & Billing

NDC Package Code
49348-921-09
Package Description
50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Code
49348-921
11-Digit Billing Format
49348092109
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
50 EA
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Sunmark Arthritis Pain Reliever
Dosage Form
-
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

Regulatory & Marketing

Labeler Name
Sunmark
FDA Application #
ANDA076200
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
04-30-2002
Listing Expiration
12-31-2019
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (49348-921). Click a package code to view its specific billing and regulatory data.

49348-921-10
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 49348-921-09 identifies a specific commercial package of 50 tablet, film coated, extended release in 1 bottle of Sunmark Arthritis Pain Reliever, labeled by Sunmark. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Sunmark on April 30, 2002. The current certification is valid through December 31, 2019.

How is this Sunmark product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49348092109. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 50 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
49348-921-09
11-Digit CMS (5-4-2)
49348-0921-09

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.