NDC Package 70518-3010-0 Latuda

View Billable Units, 11-Digit Format, RxNorm

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:
70518-3010-0
Package Description:
30 POUCH in 1 BOX / 1 TABLET, FILM COATED in 1 POUCH (70518-3010-1)
Product Code:
Proprietary Name:
Latuda
Usage Information:
This medication is used to treat certain mental/mood disorders (such as schizophrenia, depression associated with bipolar disorder). Lurasidone helps you to think more clearly, feel less nervous, and take part in everyday life. It may also help to decrease hallucinations (hearing/seeing things that are not there). In addition, this medication may improve your mood, sleep, appetite, and energy level. Lurasidone is a psychiatric medication that belongs to the class of drugs called atypical antipsychotics. It works by helping to restore the balance of certain natural substances in the brain.
11-Digit NDC Billing Format:
70518301000
NDC to RxNorm Crosswalk:
  • RxCUI: 1040041 - lurasidone HCl 80 MG Oral Tablet
  • RxCUI: 1040041 - lurasidone hydrochloride 80 MG Oral Tablet
  • RxCUI: 1040043 - Latuda 80 MG Oral Tablet
  • RxCUI: 1040043 - lurasidone hydrochloride 80 MG Oral Tablet [Latuda]
  • Labeler Name:
    Remedyrepack Inc.
    Sample Package:
    No
    Start Marketing Date:
    02-02-2021
    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 70518-3010-0?

    The NDC Packaged Code 70518-3010-0 is assigned to a package of 30 pouch in 1 box / 1 tablet, film coated in 1 pouch (70518-3010-1) of Latuda, labeled by Remedyrepack Inc.. The product's dosage form is and is administered via form.

    Is NDC 70518-3010 included in the NDC Directory?

    No, Latuda with product code 70518-3010 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Remedyrepack Inc. on February 02, 2021 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 70518-3010-0?

    The 11-digit format is 70518301000. 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
    5-4-170518-3010-05-4-270518-3010-00