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  5. NDC Package Code: 78670-140-02 Zimhi

NDC Package 78670-140-02 Zimhi

Naloxone Hydrochloride Injection, Solution Intramuscular; Subcutaneous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    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:
78670-140-02
Package Description:
2 CASE in 1 CARTON / 1 SYRINGE in 1 CASE (78670-140-11) / .5 mL in 1 SYRINGE
Product Code:
78670-140
Proprietary Name:
Zimhi
Non-Proprietary Name:
Naloxone Hydrochloride
Substance Name:
Naloxone Hydrochloride
Usage Information:
ZIMHI™ is indicated in adults and pediatric patients for:the emergency treatment of known or suspected opioid overdose, as manifested by respiratory and/or central nervous system depression.ZIMHI is intended for immediate administration as emergency therapy in settings where opioids may be present.ZIMHI is not a substitute for emergency medical care.
11-Digit NDC Billing Format:
78670014002
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 2589612 - naloxone HCL 5 MG in 0.5 ML Prefilled Syringe
  • RxCUI: 2589612 - 0.5 ML naloxone hydrochloride 10 MG/ML Prefilled Syringe
  • RxCUI: 2589612 - naloxone HCL 5 MG per 0.5 ML Prefilled Syringe
  • RxCUI: 2589618 - ZIMHI 5 MG in 0.5 ML Prefilled Syringe
  • RxCUI: 2589618 - 0.5 ML naloxone hydrochloride 10 MG/ML Prefilled Syringe [Zimhi]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Uswm, Llc
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Intramuscular - Administration within a muscle.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
    • Active Ingredient(s):
  • NALOXONE HYDROCHLORIDE 5 mg/.5mL
    • Pharmacologic Class(es):
  • Opioid Antagonist - [EPC] (Established Pharmacologic Class)
  • Opioid Antagonists - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    NDA212854
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    03-31-2022
    Listing Expiration Date:
    12-31-2024
    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.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 78670-140-02 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    78670014002J2311Inj, naloxone hcl (zimhi)1 MG0.52510

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 78670-140-02?

    The NDC Packaged Code 78670-140-02 is assigned to a package of 2 case in 1 carton / 1 syringe in 1 case (78670-140-11) / .5 ml in 1 syringe of Zimhi, a human prescription drug labeled by Uswm, Llc. The product's dosage form is injection, solution and is administered via intramuscular; subcutaneous form.

    Is NDC 78670-140 included in the NDC Directory?

    Yes, Zimhi with product code 78670-140 is active and included in the NDC Directory. The product was first marketed by Uswm, Llc on March 31, 2022 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 78670-140-02?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 78670-140-02?

    The 11-digit format is 78670014002. 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
    5-3-278670-140-025-4-278670-0140-02