NDC Package 61919-074-90 Diclofenac Sodium D/r

View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing expired due to lack of listing certification.

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:

61919-074-90

Package Description:

90 TABLET, DELAYED RELEASE in 1 BOTTLE

Product Code:

61919-074

Proprietary Name:

Diclofenac Sodium D/r

Usage Information:

INDICATIONS AND USAGECarefully consider the potential bene ts and risks of diclofenac sodium delayed-release tablets and other treatment options before deciding to use diclofenac. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS).Diclofenac is indicated:For relief of the signs and symptoms of osteoarthritisFor relief of the signs and symptoms of rheumatoid arthritisFor acute or long-term use in the relief of signs and symptoms of ankylosing spondylitis

11-Digit NDC Billing Format:

61919007490

NDC to RxNorm Crosswalk:

RxCUI: 855906 - diclofenac sodium 50 MG Delayed Release Oral Tablet
RxCUI: 855926 - diclofenac sodium 75 MG Delayed Release Oral Tablet

Labeler Name:

Direct Rx

Sample Package:

FDA Application Number:

ANDA075185

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

01-01-2014

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

61919 - Direct Rx
- 61919-074 - Diclofenac Sodium D/r
  - 61919-074-90 - 90 TABLET, DELAYED RELEASE in 1 BOTTLE

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 Code	Package Description
61919-074-30	30 TABLET, DELAYED RELEASE in 1 BOTTLE
61919-074-60	60 TABLET, DELAYED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 61919-074-90?

The NDC Packaged Code 61919-074-90 is assigned to a package of 90 tablet, delayed release in 1 bottle of Diclofenac Sodium D/r, labeled by Direct Rx. The product's dosage form is and is administered via form.

Is NDC 61919-074 included in the NDC Directory?

No, Diclofenac Sodium D/r with product code 61919-074 is excluded from the NDC Directory because it's listing has EXPIRED due to lack of listing certification. The product was first marketed by Direct Rx on January 01, 2014 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 61919-074-90?

The 11-digit format is 61919007490. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	61919-074-90	5-4-2	61919-0074-90

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