NDC Package 68210-4126-1 Loratadine

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:
68210-4126-1
Package Description:
365 TABLET in 1 PACKAGE
Product Code:
Proprietary Name:
Loratadine
Usage Information:
This medication is an antihistamine that treats symptoms such as itching, runny nose, watery eyes, and sneezing from "hay fever" and other allergies. It is also used to relieve itching from hives. Loratadine does not prevent hives or prevent/treat a serious allergic reaction (anaphylaxis). Therefore, if your doctor has prescribed epinephrine to treat allergic reactions, always carry your epinephrine injector with you. Do not use loratadine in place of your epinephrine. If you are self-treating with this medication, it is important to read the manufacturer's package instructions carefully so you know when to consult your doctor or pharmacist. (See also Precautions section.) If you are using the tablets or capsules, do not use in children younger than 6 years unless directed by the doctor. If you are using the liquid or chewable tablets, do not use in children younger than 2 years unless directed by the doctor.
11-Digit NDC Billing Format:
68210412601
NDC to RxNorm Crosswalk:
  • RxCUI: 311372 - loratadine 10 MG 24HR Oral Tablet
  • RxCUI: 311372 - loratadine 10 MG Oral Tablet
  • RxCUI: 311372 - loratadine 10 MG 24 HR Oral Tablet
  • Labeler Name:
    Spirit Pharmaceuticals Llc
    Sample Package:
    No
    Start Marketing Date:
    04-07-2021
    Listing Expiration Date:
    12-31-2023
    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 68210-4126-1?

    The NDC Packaged Code 68210-4126-1 is assigned to a package of 365 tablet in 1 package of Loratadine, labeled by Spirit Pharmaceuticals Llc. The product's dosage form is and is administered via form.

    Is NDC 68210-4126 included in the NDC Directory?

    No, Loratadine with product code 68210-4126 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Spirit Pharmaceuticals Llc on April 07, 2021 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68210-4126-1?

    The 11-digit format is 68210412601. 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
    5-4-168210-4126-15-4-268210-4126-01