NDC Package 47682-913-46 Medi First Plus Allergy Relief

Loratadine Tablet, Film Coated 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:
47682-913-46
Package Description:
1 TABLET, FILM COATED in 1 PACKET
Product Code:
Proprietary Name:
Medi First Plus Allergy Relief
Non-Proprietary Name:
Loratadine
Substance Name:
Loratadine
Usage Information:
This medication is an antihistamine that treats symptoms such as itching, runny nose, watery eyes, and sneezing from "hay fever" and other allergies. It is also used to relieve itching from hives. Loratadine does not prevent hives or prevent/treat a serious allergic reaction (anaphylaxis). Therefore, if your doctor has prescribed epinephrine to treat allergic reactions, always carry your epinephrine injector with you. Do not use loratadine in place of your epinephrine. If you are self-treating with this medication, it is important to read the manufacturer's package instructions carefully so you know when to consult your doctor or pharmacist. (See also Precautions section.) If you are using the tablets or capsules, do not use in children younger than 6 years unless directed by the doctor. If you are using the liquid or chewable tablets, do not use in children younger than 2 years unless directed by the doctor.
11-Digit NDC Billing Format:
47682091346
NDC to RxNorm Crosswalk:
  • RxCUI: 1020126 - Loradamed 10 MG 24HR Oral Tablet
  • RxCUI: 1020126 - loratadine 10 MG Oral Tablet [Loradamed]
  • RxCUI: 1020126 - Loradamed 10 MG Oral Tablet
  • RxCUI: 311372 - loratadine 10 MG 24HR Oral Tablet
  • RxCUI: 311372 - loratadine 10 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Unifirst First Aid Corporation
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA076134
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-23-2019
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    47682-913-33100 PACKET in 1 BOX / 1 TABLET, FILM COATED in 1 PACKET

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 47682-913-46?

    The NDC Packaged Code 47682-913-46 is assigned to a package of 1 tablet, film coated in 1 packet of Medi First Plus Allergy Relief, a human over the counter drug labeled by Unifirst First Aid Corporation. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 47682-913 included in the NDC Directory?

    Yes, Medi First Plus Allergy Relief with product code 47682-913 is active and included in the NDC Directory. The product was first marketed by Unifirst First Aid Corporation on April 23, 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 47682-913-46?

    The 11-digit format is 47682091346. 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
    5-3-247682-913-465-4-247682-0913-46