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  5. NDC Package Code: 51655-078-53 Hydroxyzine Hydrochloride

NDC Package 51655-078-53 Hydroxyzine Hydrochloride

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:
51655-078-53
Package Description:
10 TABLET in 1 BOTTLE, DISPENSING
Product Code:
51655-078
Proprietary Name:
Hydroxyzine Hydrochloride
Usage Information:
For symptomatic relief of anxiety and tension associated with psychoneurosis and as an adjunct in organic disease states in which anxiety is manifested.Useful in the management of pruritus due to allergic conditions such as chronic urticaria and atopic and contact dermatoses, and in histamine-mediated pruritus.As a sedative when used as a premedication and following general anesthesia, hydrOXYzine may potentiate meperidine and barbiturates, so their use in pre-anesthetic adjunctive therapy should be modified on an individual basis. Atropine and other belladonna alkaloids are not affected by the drug. HydrOXYzine is not known to interfere with the action of digitalis in any way and it may be used concurrently with this agent.The effectiveness of hydrOXYzine as an antianxiety agent for long term use, that is more than 4 months, has not been assessed by systematic clinical studies. The physician should reassess periodically the usefulness of the drug for the individual patient.
11-Digit NDC Billing Format:
51655007853
NDC to RxNorm Crosswalk:
  • RxCUI: 995218 - hydrOXYzine HCl 10 MG Oral Tablet
  • RxCUI: 995218 - hydroxyzine hydrochloride 10 MG Oral Tablet
    • Labeler Name:
    Northwind Pharmaceuticals, Llc
    Sample Package:
    No
    Start Marketing Date:
    09-15-2014
    Listing Expiration Date:
    12-31-2019
    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 51655-078-53?

    The NDC Packaged Code 51655-078-53 is assigned to a package of 10 tablet in 1 bottle, dispensing of Hydroxyzine Hydrochloride, labeled by Northwind Pharmaceuticals, Llc. The product's dosage form is and is administered via form.

    Is NDC 51655-078 included in the NDC Directory?

    No, Hydroxyzine Hydrochloride with product code 51655-078 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Northwind Pharmaceuticals, Llc on September 15, 2014 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 51655-078-53?

    The 11-digit format is 51655007853. 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
    5-3-251655-078-535-4-251655-0078-53