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  5. NDC Package Code: 70860-751-02 Famotidine

NDC Package 70860-751-02 Famotidine

Injection, Solution Intravenous - 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:
70860-751-02
Package Description:
25 VIAL, SINGLE-DOSE in 1 CARTON / 2 mL in 1 VIAL, SINGLE-DOSE (70860-751-41)
Product Code:
70860-751
Proprietary Name:
Famotidine
Non-Proprietary Name:
Famotidine
Substance Name:
Famotidine
Usage Information:
Famotidine is used to treat ulcers of the stomach and intestines and to prevent intestinal ulcers from coming back after they have healed. This medication is also used to treat certain stomach and throat (esophagus) problems (such as erosive esophagitis, gastroesophageal reflux disease-GERD, Zollinger-Ellison syndrome). It works by decreasing the amount of acid your stomach makes. It relieves symptoms such as cough that doesn't go away, stomach pain, heartburn, and difficulty swallowing. Famotidine belongs to a class of drugs known as H2 blockers. This medication is also available without a prescription. It is used to prevent and treat heartburn and other symptoms caused by too much acid in the stomach (acid indigestion). If you are taking this medication for self-treatment, it is important to read the manufacturer's package instructions carefully so you know when to consult your doctor or pharmacist.
11-Digit NDC Billing Format:
70860075102
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1743833 - famotidine 20 MG in 2 ML Injection
  • RxCUI: 1743833 - 2 ML famotidine 10 MG/ML Injection
  • RxCUI: 1743833 - famotidine 20 MG per 2 ML Injection
  • RxCUI: 204441 - famotidine 10 MG/ML Injectable Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Athenex Pharmaceutical Division, 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):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • FAMOTIDINE 10 mg/mL
    • Pharmacologic Class(es):
  • Histamine H2 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Histamine-2 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA075622
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-10-2020
    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.

    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 70860-751-02 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    70860075102Famotidine10 MG225250

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70860-751-02?

    The NDC Packaged Code 70860-751-02 is assigned to a package of 25 vial, single-dose in 1 carton / 2 ml in 1 vial, single-dose (70860-751-41) of Famotidine, a human prescription drug labeled by Athenex Pharmaceutical Division, Llc.. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 70860-751 included in the NDC Directory?

    Yes, Famotidine with product code 70860-751 is active and included in the NDC Directory. The product was first marketed by Athenex Pharmaceutical Division, Llc. on August 10, 2020 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 NDC billing unit for package 70860-751-02?

    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 70860-751-02?

    The 11-digit format is 70860075102. 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
    5-3-270860-751-025-4-270860-0751-02