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  5. NDC Package Code: 71205-316-01 Medique Diamode

NDC Package 71205-316-01 Medique Diamode

Loperamide Hydrochloride 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:
71205-316-01
Package Description:
1 TABLET in 1 PACKET
Product Code:
71205-316
Proprietary Name:
Medique Diamode
Non-Proprietary Name:
Loperamide Hydrochloride
Substance Name:
Loperamide Hydrochloride
Usage Information:
•drink plenty of clear fluids to help prevent dehydration caused by diarrheaAdults and children (12 years and over): Take 2 caplets after the first loose stool; 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:
71205031601
Product Type:
Human Otc Drug
Labeler Name:
Proficient Rx Lp
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):
  • Opioid Agonist - [EPC] (Established Pharmacologic Class)
  • Opioid Agonists - [MoA] (Mechanism of Action)
    • 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:
    12-31-2025
    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
    71205-316-066 TABLET in 1 PACKET

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 71205-316-01?

    The NDC Packaged Code 71205-316-01 is assigned to a package of 1 tablet in 1 packet of Medique Diamode, a human over the counter drug labeled by Proficient Rx Lp. The product's dosage form is tablet and is administered via oral form.

    Is NDC 71205-316 included in the NDC Directory?

    Yes, Medique Diamode with product code 71205-316 is active and included in the NDC Directory. The product was first marketed by Proficient Rx Lp on December 30, 2008 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 71205-316-01?

    The 11-digit format is 71205031601. 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
    5-3-271205-316-015-4-271205-0316-01