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  5. NDC Package Code: 0185-0687-10 Etodolac

NDC Package 0185-0687-10 Etodolac

Tablet, Coated Oral - 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 approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

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:
0185-0687-10
Package Description:
1000 TABLET, COATED in 1 BOTTLE
Product Code:
0185-0687
Proprietary Name:
Etodolac
Non-Proprietary Name:
Etodolac
Substance Name:
Etodolac
Usage Information:
Etodolac is used to relieve pain from various conditions. It also reduces pain, swelling, and joint stiffness from arthritis. This medication is known as a nonsteroidal anti-inflammatory drug (NSAID). It works by blocking your body's production of certain natural substances that cause inflammation. If you are treating a chronic condition such as arthritis, ask your doctor about non-drug treatments and/or using other medications to treat your pain. See also Warning section.
11-Digit NDC Billing Format:
00185068710
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Eon Labs, Inc.
Dosage Form:
Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
ETODOLAC 500 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA074903
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
04-20-2015
End Marketing Date:
07-31-2025
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
0185-0687-01100 TABLET, COATED in 1 BOTTLE
0185-0687-05500 TABLET, COATED in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0185-0687-10?

The NDC Packaged Code 0185-0687-10 is assigned to a package of 1000 tablet, coated in 1 bottle of Etodolac, a human prescription drug labeled by Eon Labs, Inc.. The product's dosage form is tablet, coated and is administered via oral form.

Is NDC 0185-0687 included in the NDC Directory?

Yes, Etodolac with product code 0185-0687 is active and included in the NDC Directory. The product was first marketed by Eon Labs, Inc. on April 20, 2015.

What is the 11-digit format for NDC 0185-0687-10?

The 11-digit format is 00185068710. 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 4-4-2 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
4-4-20185-0687-105-4-200185-0687-10