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  5. NDC Package Code: 70518-0091-2 Kaletra

NDC Package 70518-0091-2 Kaletra

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 because the listing data was inactivated by the FDA.

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:
70518-0091-2
Package Description:
30 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
70518-0091
Proprietary Name:
Kaletra
Usage Information:
This combination product contains two medications: lopinavir and ritonavir. This product 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 lopinavir and ritonavir belong to a class of drugs known as HIV protease inhibitors. Ritonavir increases ("boosts") the levels of lopinavir. This helps lopinavir work better. Lopinavir/ritonavir 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:
70518009102
NDC to RxNorm Crosswalk:
  • RxCUI: 597730 - lopinavir 200 MG / ritonavir 50 MG Oral Tablet
  • RxCUI: 847741 - Kaletra 200 MG / 50 MG Oral Tablet
  • RxCUI: 847741 - lopinavir 200 MG / ritonavir 50 MG Oral Tablet [Kaletra]
    • Labeler Name:
    Remedyrepack Inc.
    Sample Package:
    No
    Start Marketing Date:
    12-29-2016
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I
    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 70518-0091-2?

    The NDC Packaged Code 70518-0091-2 is assigned to a package of 30 tablet, film coated in 1 blister pack of Kaletra, labeled by Remedyrepack Inc.. The product's dosage form is and is administered via form.

    Is NDC 70518-0091 included in the NDC Directory?

    No, Kaletra with product code 70518-0091 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Remedyrepack Inc. on December 29, 2016 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70518-0091-2?

    The 11-digit format is 70518009102. 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
    5-4-170518-0091-25-4-270518-0091-02