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  5. NDC Package Code: 70710-1727-9 Tofacitinib

NDC Package 70710-1727-9 Tofacitinib

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 discontinued by the firm.

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:
70710-1727-9
Package Description:
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Code:
70710-1727
Proprietary Name:
Tofacitinib
Usage Information:
Rheumatoid ArthritisTofacitinib extended-release tablets are indicated for the treatment of adult patients with moderately to severely active rheumatoid arthritis (RA) who have had an inadequate response or intolerance to methotrexate. It may be used as monotherapy or in combination with methotrexate or other nonbiologic disease-modifying antirheumatic drugs (DMARDs).Limitations of Use:Use of tofacitinib extended-release tablets in combination with biologic DMARDs or with potent immunosuppressants such as azathioprine and cyclosporine is not recommended.Psoriatic ArthritisTofacitinib extended-release tablets are indicated for the treatment of adult patients with active psoriatic arthritis (PsA) who have had an inadequate response or intolerance to methotrexate or other disease-modifying antirheumatic drugs (DMARDs).Limitations of Use:Use of tofacitinib extended-release tablets in combination with biologic DMARDs or with potent immunosuppressants such as azathioprine and cyclosporine is not recommended.Ulcerative ColitisTofacitinib extended-release tablets are indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (UC), who have an inadequate response or who are intolerant to TNF blockers. Limitations of Use:Use of tofacitinib extended-release tablets in combination with biological therapies for UC or with potent immunosuppressants such as azathioprine and cyclosporine is not recommended.
11-Digit NDC Billing Format:
70710172709
Labeler Name:
Zydus Pharmaceuticals Usa Inc.
Sample Package:
No
FDA Application Number:
ANDA214264
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
03-12-2025
End Marketing Date:
05-14-2025
Listing Expiration Date:
05-14-2025
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
70710-1727-330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 70710-1727-9?

The NDC Packaged Code 70710-1727-9 is assigned to a package of 90 tablet, film coated, extended release in 1 bottle of Tofacitinib, labeled by Zydus Pharmaceuticals Usa Inc.. The product's dosage form is and is administered via form.

Is NDC 70710-1727 included in the NDC Directory?

No, Tofacitinib with product code 70710-1727 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Zydus Pharmaceuticals Usa Inc. on March 12, 2025 and its listing in the NDC Directory is set to expire on May 14, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70710-1727-9?

The 11-digit format is 70710172709. 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 5-4-1 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
5-4-170710-1727-95-4-270710-1727-09