NDC Package 70771-1860-8 Zituvimet

Sitagliptin And Metformin Hydrochloride Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

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:
70771-1860-8
Package Description:
180 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Zituvimet
Non-Proprietary Name:
Sitagliptin And Metformin Hydrochloride
Substance Name:
Metformin Hydrochloride; Sitagliptin
11-Digit NDC Billing Format:
70771186008
NDC to RxNorm Crosswalk:
  • RxCUI: 2677162 - Zituvimet 50 MG / 1000 MG Oral Tablet
  • RxCUI: 2677162 - metformin hydrochloride 1000 MG / sitagliptin 50 MG Oral Tablet [Zituvimet]
  • RxCUI: 2677164 - Zituvimet 50 MG / 500 MG Oral Tablet
  • RxCUI: 2677164 - metformin hydrochloride 500 MG / sitagliptin 50 MG Oral Tablet [Zituvimet]
  • RxCUI: 861769 - SITagliptin 50 MG / metFORMIN HCl 1000 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Zydus Lifesciences Limited
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    NDA216743
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    03-14-2024
    Listing Expiration Date:
    12-31-2025
    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
    70771-1860-660 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70771-1860-8?

    The NDC Packaged Code 70771-1860-8 is assigned to a package of 180 tablet, film coated in 1 bottle of Zituvimet, a human prescription drug labeled by Zydus Lifesciences Limited. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 70771-1860 included in the NDC Directory?

    Yes, Zituvimet with product code 70771-1860 is active and included in the NDC Directory. The product was first marketed by Zydus Lifesciences Limited on March 14, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70771-1860-8?

    The 11-digit format is 70771186008. 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
    5-4-170771-1860-85-4-270771-1860-08