NDC Package 49035-208-04 Childrens Allergy

Fexofenadine Hcl Suspension 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:
49035-208-04
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 118 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Childrens Allergy
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:
49035020804
NDC to RxNorm Crosswalk:
  • RxCUI: 997491 - fexofenadine HCl 30 MG in 5 mL Oral Suspension
  • RxCUI: 997491 - fexofenadine hydrochloride 6 MG/ML Oral Suspension
  • RxCUI: 997491 - fexofenadine HCl 30 MG per 5 ML Oral Suspension
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Equate (wal-mart Stores, Inc.) (see Also Wal-mart Inc)
    Dosage Form:
    Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA203330
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-01-2020
    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 49035-208-04?

    The NDC Packaged Code 49035-208-04 is assigned to a package of 1 bottle, plastic in 1 carton / 118 ml in 1 bottle, plastic of Childrens Allergy, a human over the counter drug labeled by Equate (wal-mart Stores, Inc.) (see Also Wal-mart Inc). The product's dosage form is suspension and is administered via oral form.

    Is NDC 49035-208 included in the NDC Directory?

    Yes, Childrens Allergy with product code 49035-208 is active and included in the NDC Directory. The product was first marketed by Equate (wal-mart Stores, Inc.) (see Also Wal-mart Inc) on July 01, 2020 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 49035-208-04?

    The 11-digit format is 49035020804. 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
    5-3-249035-208-045-4-249035-0208-04