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  5. NDC Package Code: 47682-021-25 Private Label Distributor

NDC Package 47682-021-25 Private Label Distributor

Loperamide Hcl 2 Mg Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
47682-021-25
Package Description:
25 PACKET in 1 BOX, UNIT-DOSE / 1 TABLET in 1 PACKET
Product Code:
47682-021
Proprietary Name:
Private Label Distributor
Non-Proprietary Name:
Loperamide Hcl 2 Mg
Substance Name:
Loperamide Hydrochloride
Usage Information:
Do not use more than directed drink plenty of clear fluids to help prevent dehydration caused by diarrhea Adults and children (12 years and older): Take 2 caplets after the first loose stool followed by 1 caplet after each subsequent loose stool but no more than 4 caplets in 24 hours. Children under 12 years: Do not give to children under 12 years of age.
11-Digit NDC Billing Format:
47682002125
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Unifirst First Aid Corporation
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
LOPERAMIDE HYDROCHLORIDE 2 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA074091
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
12-30-2008
Listing Expiration Date:
12-31-2026
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
47682-021-3030 PACKET in 1 BOX, UNIT-DOSE / 1 TABLET in 1 PACKET
47682-021-5050 PACKET in 1 BOX, UNIT-DOSE / 1 TABLET in 1 PACKET
47682-021-7575 PACKET in 1 BOX, UNIT-DOSE / 1 TABLET in 1 PACKET

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 47682-021-25?

The NDC Packaged Code 47682-021-25 is assigned to a package of 25 packet in 1 box, unit-dose / 1 tablet in 1 packet of Private Label Distributor, a human over the counter drug labeled by Unifirst First Aid Corporation. The product's dosage form is tablet and is administered via oral form.

Is NDC 47682-021 included in the NDC Directory?

Yes, Private Label Distributor with product code 47682-021 is active and included in the NDC Directory. The product was first marketed by Unifirst First Aid Corporation on December 30, 2008 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 47682-021-25?

The 11-digit format is 47682002125. 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
5-3-247682-021-255-4-247682-0021-25