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  5. NDC Package Code: 49702-258-37 Triumeq Pd

NDC Package 49702-258-37 Triumeq Pd

Abacavir Sulfate,Dolutegravir Sodium,Lamivudine Kit - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
49702-258-37
Package Description:
1 KIT in 1 CARTON * 90 TABLET, FILM COATED in 1 BOTTLE (49702-272-59)
Product Code:
49702-258
Proprietary Name:
Triumeq Pd
Non-Proprietary Name:
Abacavir Sulfate, Dolutegravir Sodium, Lamivudine
Usage Information:
TRIUMEQ is indicated for the treatment of human immunodeficiency virus type 1 (HIV-1) infection in adults and in pediatric patients weighing at least 40 kg.Limitations of Use:•TRIUMEQ alone is not recommended in patients with resistance-associated integrase substitutions or clinically suspected integrase strand transfer inhibitor resistance because the dose of dolutegravir in TRIUMEQ is insufficient in these subpopulations. See full prescribing information for TIVICAY (dolutegravir).
11-Digit NDC Billing Format:
49702025837
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Product Type:
Human Prescription Drug
Labeler Name:
Viiv Healthcare Company
Dosage Form:
Kit - A packaged collection of related material.
Sample Package:
No
FDA Application Number:
NDA215413
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
03-30-2022
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.

Frequently Asked Questions

What is NDC 49702-258-37?

The NDC Packaged Code 49702-258-37 is assigned to a package of 1 kit in 1 carton * 90 tablet, film coated in 1 bottle (49702-272-59) of Triumeq Pd, a human prescription drug labeled by Viiv Healthcare Company. The product's dosage form is kit and is administered via form.

Is NDC 49702-258 included in the NDC Directory?

Yes, Triumeq Pd with product code 49702-258 is active and included in the NDC Directory. The product was first marketed by Viiv Healthcare Company on March 30, 2022 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 NDC billing unit for package 49702-258-37?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units.

What is the 11-digit format for NDC 49702-258-37?

The 11-digit format is 49702025837. 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
5-3-249702-258-375-4-249702-0258-37