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  5. NDC Package Code: 72089-307-15 Gimoti

NDC Package 72089-307-15 Gimoti

Metoclopramide Hydrochloride Spray Nasal - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
72089-307-15
Package Description:
1 BOTTLE, PUMP in 1 CARTON / 9.8 mL in 1 BOTTLE, PUMP
Product Code:
72089-307
Proprietary Name:
Gimoti
Non-Proprietary Name:
Metoclopramide Hydrochloride
Substance Name:
Metoclopramide Hydrochloride
Usage Information:
GIMOTI is indicated for the relief of symptoms in adults with acute and recurrent diabetic gastroparesis.
11-Digit NDC Billing Format:
72089030715
NDC to RxNorm Crosswalk:
  • RxCUI: 2380564 - metoclopramide 15 MG/ACTUAT Nasal Spray
  • RxCUI: 2380564 - metoclopramide 15 MG/ACTUAT (equivalent to 17.73 MG/ACTUAT of metoclopramide HCl) Nasal Spray
  • RxCUI: 2380570 - Gimoti 15 MG/ACTUAT Nasal Spray
  • RxCUI: 2380570 - metoclopramide 15 MG/ACTUAT Nasal Spray [Gimoti]
  • RxCUI: 2380570 - Gimoti 15 MG/ACTUAT (equivalent to 17.73 MG/ACTUAT of metoclopramide HCl) Nasal Spray
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Evoke Pharma, Inc.
    Dosage Form:
    Spray - A liquid minutely divided as by a jet of air or steam.
    Administration Route(s):
  • Nasal - Administration to the nose; administered by way of the nose.
    • Active Ingredient(s):
  • METOCLOPRAMIDE HYDROCHLORIDE 15 mg/.07mL
    • Pharmacologic Class(es):
  • Dopamine D2 Antagonists - [MoA] (Mechanism of Action)
  • Dopamine-2 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    NDA209388
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    06-19-2020
    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.

    Frequently Asked Questions

    What is NDC 72089-307-15?

    The NDC Packaged Code 72089-307-15 is assigned to a package of 1 bottle, pump in 1 carton / 9.8 ml in 1 bottle, pump of Gimoti, a human prescription drug labeled by Evoke Pharma, Inc.. The product's dosage form is spray and is administered via nasal form.

    Is NDC 72089-307 included in the NDC Directory?

    Yes, Gimoti with product code 72089-307 is active and included in the NDC Directory. The product was first marketed by Evoke Pharma, Inc. on June 19, 2020 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 11-digit format for NDC 72089-307-15?

    The 11-digit format is 72089030715. 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
    5-3-272089-307-155-4-272089-0307-15