NDC Package 10202-107-10 Allergy

Fexofenadine Hydrochloride Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

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:
10202-107-10
Package Description:
2 BLISTER PACK in 1 CARTON / 5 TABLET in 1 BLISTER PACK
Product Code:
Proprietary Name:
Allergy
Non-Proprietary Name:
Fexofenadine Hydrochloride
Substance Name:
Fexofenadine Hydrochloride
Usage Information:
Adults and children 12 years of age and over         take one 180 mg tablet with water once a day; do not take more than 1 tablet in 24 hourschildren under 12 years of agedo not useadults 65 years of age  and olderask a doctorconsumers with kidney diseaseask a doctor
11-Digit NDC Billing Format:
10202010710
NDC to RxNorm Crosswalk:
  • RxCUI: 997420 - fexofenadine HCl 180 MG 24 HR Oral Tablet
  • RxCUI: 997420 - fexofenadine hydrochloride 180 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    7-eleven
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA076502
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-15-2019
    Listing Expiration Date:
    12-31-2024
    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 10202-107-10?

    The NDC Packaged Code 10202-107-10 is assigned to a package of 2 blister pack in 1 carton / 5 tablet in 1 blister pack of Allergy, a human over the counter drug labeled by 7-eleven. The product's dosage form is tablet and is administered via oral form.

    Is NDC 10202-107 included in the NDC Directory?

    Yes, Allergy with product code 10202-107 is active and included in the NDC Directory. The product was first marketed by 7-eleven on November 15, 2019 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 10202-107-10?

    The 11-digit format is 10202010710. 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
    5-3-210202-107-105-4-210202-0107-10