NDC Package 72090-061-90 Fex-allergy Relief

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:
72090-061-90
Package Description:
90 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Fex-allergy Relief
Usage Information:
Adults and children 12 years of age and overTake one 180 mg tablet with water once a day; do not take more than 1 tablets in 24 hours.children 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:
72090006190
NDC to RxNorm Crosswalk:
  • RxCUI: 997420 - fexofenadine HCl 180 MG 24 HR Oral Tablet
  • RxCUI: 997420 - fexofenadine hydrochloride 180 MG Oral Tablet
  • Labeler Name:
    Pioneer Life Sciences, Llc
    Sample Package:
    No
    Start Marketing Date:
    09-21-2020
    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 72090-061-90?

    The NDC Packaged Code 72090-061-90 is assigned to a package of 90 tablet in 1 bottle of Fex-allergy Relief, labeled by Pioneer Life Sciences, Llc. The product's dosage form is and is administered via form.

    Is NDC 72090-061 included in the NDC Directory?

    No, Fex-allergy Relief with product code 72090-061 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Pioneer Life Sciences, Llc on September 21, 2020 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 72090-061-90?

    The 11-digit format is 72090006190. 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
    5-3-272090-061-905-4-272090-0061-90