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  5. NDC Package Code: 17856-1823-1 Qdryl Allergy

NDC Package 17856-1823-1 Qdryl Allergy

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
17856-1823-1
Package Description:
10 mL in 1 CUP, UNIT-DOSE
Product Code:
17856-1823
Proprietary Name:
Qdryl Allergy
Usage Information:
Use an accurate measuring device to administer this medicationtake every 4 to 6 hourschildren under 2 yearsdo not usechildren 2 to 5 yearsask a doctorchildren 6 years to under 12 years5 mL (1 tsp) to 10 mL (2 tsp); not more than 60 mL (12 tsp) in 24 hoursadults and children 12 years and over10 mL (2 tsp) to 20 mL (4 tsp); not more than 120 mL (24 tsp) in 24 hours
11-Digit NDC Billing Format:
17856182301
NDC to RxNorm Crosswalk:
  • RxCUI: 1049906 - diphenhydrAMINE HCl 12.5 MG in 5 mL Oral Solution
  • RxCUI: 1049906 - diphenhydramine hydrochloride 2.5 MG/ML Oral Solution
  • RxCUI: 1049906 - diphenhydramine HCl 12.5 MG per 5 ML Oral Solution
  • RxCUI: 1049906 - diphenhydramine hydrochloride 25 MG per 10 ML Oral Solution
  • RxCUI: 1049906 - diphenhydramine hydrochloride 50 MG per 20 ML Oral Solution
    • Labeler Name:
    Atlantic Biologicals Corp
    Sample Package:
    No
    Start Marketing Date:
    12-01-1997
    Listing Expiration Date:
    12-31-2018
    Exclude Flag:
    I
    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 17856-1823-1?

    The NDC Packaged Code 17856-1823-1 is assigned to a package of 10 ml in 1 cup, unit-dose of Qdryl Allergy, labeled by Atlantic Biologicals Corp. The product's dosage form is and is administered via form.

    Is NDC 17856-1823 included in the NDC Directory?

    No, Qdryl Allergy with product code 17856-1823 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Atlantic Biologicals Corp on December 01, 1997 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 17856-1823-1?

    The 11-digit format is 17856182301. 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 5-4-1 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
    5-4-117856-1823-15-4-217856-1823-01