NDC Package 0781-7176-12 Naloxone Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

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:
0781-7176-12
Package Description:
2 VIAL, SINGLE-DOSE in 1 CARTON / .1 mL in 1 VIAL, SINGLE-DOSE (0781-7176-06)
Product Code:
Proprietary Name:
Naloxone Hydrochloride
Usage Information:
Naloxone HCl Nasal Spray is indicated for the emergency treatment of known or suspected opioid overdose, as manifested by respiratory and/or central nervous system depression.Naloxone HCl Nasal Spray is intended for immediate administration as emergency therapy in settings where opioids may be present.Naloxone HCl Nasal Spray is not a substitute for emergency medical care.
11-Digit NDC Billing Format:
00781717612
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1725059 - naloxone HCl 4 MG per 0.1 ML Nasal Spray
  • RxCUI: 1725059 - naloxone hydrochloride 40 MG/ML Nasal Spray
  • Labeler Name:
    Sandoz Inc.
    Sample Package:
    No
    Start Marketing Date:
    12-20-2021
    Listing Expiration Date:
    12-31-2023
    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 0781-7176-12?

    The NDC Packaged Code 0781-7176-12 is assigned to a package of 2 vial, single-dose in 1 carton / .1 ml in 1 vial, single-dose (0781-7176-06) of Naloxone Hydrochloride, labeled by Sandoz Inc.. The product's dosage form is and is administered via form.

    Is NDC 0781-7176 included in the NDC Directory?

    No, Naloxone Hydrochloride with product code 0781-7176 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Sandoz Inc. on December 20, 2021 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 0781-7176-12?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

    What is the 11-digit format for NDC 0781-7176-12?

    The 11-digit format is 00781717612. 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 4-4-2 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
    4-4-20781-7176-125-4-200781-7176-12