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  5. NDC Package Code: 49349-178-02 Sulfasalazine

NDC Package 49349-178-02 Sulfasalazine

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory .

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:
49349-178-02
Package Description:
30 TABLET in 1 BLISTER PACK
Product Code:
49349-178
Proprietary Name:
Sulfasalazine
Usage Information:
Sulfasalazine is used to treat a certain type of bowel disease called ulcerative colitis. This medication does not cure this condition, but it helps decrease symptoms such as fever, stomach pain, diarrhea, and rectal bleeding. After an attack is treated, sulfasalazine is also used to increase the amount of time between attacks. This medication works by reducing irritation and swelling in the large intestines. In addition, delayed-release tablets of sulfasalazine are used to treat rheumatoid arthritis. Sulfasalazine helps to reduce joint pain, swelling, and stiffness. Early treatment of rheumatoid arthritis with sulfasalazine helps to reduce/prevent further joint damage so you can do more of your normal daily activities. This medication is used with other drugs, rest, and physical therapy in patients who have not responded to other medications (salicylates, nonsteroidal anti-inflammatory drugs-NSAIDs).
11-Digit NDC Billing Format:
49349017802
Labeler Name:
Remedyrepack Inc.
Sample Package:
No
FDA Application Number:
ANDA085828
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
04-19-2011
End Marketing Date:
04-20-2011
Listing Expiration Date:
04-20-2011
Exclude Flag:
D
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 49349-178-02?

The NDC Packaged Code 49349-178-02 is assigned to a package of 30 tablet in 1 blister pack of Sulfasalazine, labeled by Remedyrepack Inc.. The product's dosage form is and is administered via form.

Is NDC 49349-178 included in the NDC Directory?

The product was first marketed by Remedyrepack Inc. on April 19, 2011 and its listing in the NDC Directory is set to expire on April 20, 2011 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 49349-178-02?

The 11-digit format is 49349017802. 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
5-3-249349-178-025-4-249349-0178-02