NDC Package 0173-0595-02 Combivir

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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:
0173-0595-02
Package Description:
120 TABLET, FILM COATED in 1 DOSE PACK
Product Code:
Proprietary Name:
Combivir
Usage Information:
This product contains 2 drugs: lamivudine and zidovudine. It is used with other HIV medications to help control HIV infection. It helps to decrease the amount of HIV in your body so your immune system can work better. This lowers your chance of getting HIV complications (such as new infections, cancer) and improves your quality of life. Both lamivudine and zidovudine belong to a class of drugs known as nucleoside reverse transcriptase inhibitors (NRTIs). Lamivudine/zidovudine is not a cure for HIV infection. To decrease your risk of spreading HIV disease to others, do all of the following: (1) continue to take all HIV medications exactly as prescribed by your doctor, (2) always use an effective barrier method (latex or polyurethane condoms/dental dams) during all sexual activity, and (3) do not share personal items (such as needles/syringes, toothbrushes, and razors) that may have contacted blood or other body fluids. Consult your doctor or pharmacist for more details.
11-Digit NDC Billing Format:
00173059502
Labeler Name:
Glaxosmithkline Llc
Sample Package:
No
FDA Application Number:
NDA020857
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
09-30-1997
End Marketing Date:
07-31-2014
Listing Expiration Date:
07-31-2014
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.

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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
0173-0595-0060 TABLET, FILM COATED in 1 BOTTLE

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Frequently Asked Questions

What is NDC 0173-0595-02?

The NDC Packaged Code 0173-0595-02 is assigned to a package of 120 tablet, film coated in 1 dose pack of Combivir, labeled by Glaxosmithkline Llc. The product's dosage form is and is administered via form.

Is NDC 0173-0595 included in the NDC Directory?

The product was first marketed by Glaxosmithkline Llc on September 30, 1997 and its listing in the NDC Directory is set to expire on July 31, 2014 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0173-0595-02?

The 11-digit format is 00173059502. 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 4-4-2 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
4-4-20173-0595-025-4-200173-0595-02