NDC Package 56062-999-30 Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride

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:
56062-999-30
Package Description:
1 BLISTER PACK in 1 CARTON / 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product Code:
Proprietary Name:
Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
Usage Information:
Do not divide, crush, chew or dissolve the tablet; swallow tablet wholeadults and children 12 years of age and overtake 1 tablet with a glass of water every 12 hours on an empty stomach; do not take more than 2 tablets 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:
56062099930
NDC to RxNorm Crosswalk:
  • RxCUI: 997406 - fexofenadine HCl 60 MG / pseudoephedrine HCl 120 MG 12HR Extended Release Oral Tablet
  • RxCUI: 997406 - 12 HR fexofenadine hydrochloride 60 MG / pseudoephedrine hydrochloride 120 MG Extended Release Oral Tablet
  • RxCUI: 997406 - fexofenadine hydrochloride 60 MG / pseudoephedrine hydrochloride 120 MG 12 HR Extended Release Oral Tablet
  • Labeler Name:
    Publix Super Markets Inc
    Sample Package:
    No
    Start Marketing Date:
    04-01-2019
    Listing Expiration Date:
    12-31-2020
    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 56062-999-30?

    The NDC Packaged Code 56062-999-30 is assigned to a package of 1 blister pack in 1 carton / 30 tablet, film coated, extended release in 1 blister pack of Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride, labeled by Publix Super Markets Inc. The product's dosage form is and is administered via form.

    Is NDC 56062-999 included in the NDC Directory?

    No, Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride with product code 56062-999 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Publix Super Markets Inc on April 01, 2019 and its listing in the NDC Directory is set to expire on December 31, 2020 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 56062-999-30?

    The 11-digit format is 56062099930. 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
    5-3-256062-999-305-4-256062-0999-30