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  5. NDC Package Code: 0703-4502-04 Metoclopramide

NDC Package 0703-4502-04 Metoclopramide

Injection, Solution Intramuscular; 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:
0703-4502-04
Package Description:
25 VIAL, SINGLE-USE in 1 TRAY / 2 mL in 1 VIAL, SINGLE-USE (0703-4502-01)
Product Code:
0703-4502
Proprietary Name:
Metoclopramide
Non-Proprietary Name:
Metoclopramide
Substance Name:
Metoclopramide Hydrochloride
Usage Information:
Metoclopramide should not be used whenever stimulation of gastrointestinal motility might be dangerous, e.g., in the presence of gastrointestinal hemorrhage, mechanical obstruction, or perforation. Metoclopramide is contraindicated in patients with pheochromocytoma because the drug may cause a hypertensive crisis, probably due to release of catecholamines from the tumor. Such hypertensive crises may be controlled by phentolamine. Metoclopramide is contraindicated in patients with known sensitivity or intolerance to the drug. Metoclopramide should not be used in epileptics or patients receiving other drugs which are likely to cause extrapyramidal reactions, since the frequency and severity of seizures or extrapyramidal reactions may be increased.
11-Digit NDC Billing Format:
00703450204
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 311670 - metoclopramide 10 MG per 2 ML Injection
  • RxCUI: 311670 - 2 ML metoclopramide 5 MG/ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Teva Parenteral Medicines, Inc.
    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.
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • METOCLOPRAMIDE HYDROCHLORIDE 5 mg/mL
    • Pharmacologic Class(es):
  • Dopamine D2 Antagonists - [MoA] (Mechanism of Action)
  • Dopamine-2 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA073135
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-01-1991
    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 0703-4502-04 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    00703450204J2765Metoclopramide hcl injection10 MG225125

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0703-4502-04?

    The NDC Packaged Code 0703-4502-04 is assigned to a package of 25 vial, single-use in 1 tray / 2 ml in 1 vial, single-use (0703-4502-01) of Metoclopramide, a human prescription drug labeled by Teva Parenteral Medicines, Inc.. The product's dosage form is injection, solution and is administered via intramuscular; intravenous form.

    Is NDC 0703-4502 included in the NDC Directory?

    Yes, Metoclopramide with product code 0703-4502 is active and included in the NDC Directory. The product was first marketed by Teva Parenteral Medicines, Inc. on December 01, 1991 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 0703-4502-04?

    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 0703-4502-04?

    The 11-digit format is 00703450204. 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
    4-4-20703-4502-045-4-200703-4502-04