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  5. NDC Package Code: 59726-701-15 Iallergy Relief

NDC Package 59726-701-15 Iallergy Relief

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

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
59726-701-15
Package Description:
1 BOTTLE, PLASTIC in 1 BOX / 150 TABLET, COATED in 1 BOTTLE, PLASTIC
Product Code:
59726-701
Proprietary Name:
Iallergy Relief
Non-Proprietary Name:
Fexofenadine Hcl
Substance Name:
Fexofenadine Hydrochloride
Usage Information:
Fexofenadine is an antihistamine used to relieve allergy symptoms such as watery eyes, runny nose, itching eyes/nose, sneezing, hives, and itching. It works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction.
11-Digit NDC Billing Format:
59726070115
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:
    P & L Development, Llc
    Dosage Form:
    Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • FEXOFENADINE HYDROCHLORIDE 180 mg/1
    • Pharmacologic Class(es):
  • Histamine H1 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Histamine-1 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA204507
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-20-2021
    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 59726-701-15?

    The NDC Packaged Code 59726-701-15 is assigned to a package of 1 bottle, plastic in 1 box / 150 tablet, coated in 1 bottle, plastic of Iallergy Relief, a human over the counter drug labeled by P & L Development, Llc. The product's dosage form is tablet, coated and is administered via oral form.

    Is NDC 59726-701 included in the NDC Directory?

    Yes, Iallergy Relief with product code 59726-701 is active and included in the NDC Directory. The product was first marketed by P & L Development, Llc on August 20, 2021 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 59726-701-15?

    The 11-digit format is 59726070115. 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
    5-3-259726-701-155-4-259726-0701-15