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  5. NDC Package Code: 62559-190-16 Metoclopramide

NDC Package 62559-190-16 Metoclopramide

Solution Oral - 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:
62559-190-16
Package Description:
473 mL in 1 BOTTLE, PLASTIC
Product Code:
62559-190
Proprietary Name:
Metoclopramide
Non-Proprietary Name:
Metoclopramide
Substance Name:
Metoclopramide Hydrochloride
Usage Information:
The use of Metoclopramide Oral Solution is recommended for adults only. Therapy should not exceed 12 weeks in duration.Symptomatic Gastroesophageal RefluxMetoclopramide Oral Solution is indicated as short-term (4 to 12 weeks) therapy for adults with symptomatic, documented gastroesophageal reflux who fail to respond to conventional therapy.The principal effect of metoclopramide is on symptoms of post-prandial and daytime heartburn with less observed effect on nocturnal symptoms. If symptoms are confined to particular situations, such as following the evening meal, use of metoclopramide as single doses prior to the provocative situation should be considered, rather than using the drug throughout the day. Healing of esophageal ulcers and erosions has been endoscopically demonstrated at the end of 12-week trial using doses of 15 mg 4 times daily. As there is no documented correlation between symptoms and healing of esophageal lesions, patients with documented lesions should be monitored endoscopically.Diabetic Gastroparesis (Diabetic Gastric Stasis)Metoclopramide is indicated for the relief of symptoms associated with acute and recurrent diabetic gastric stasis. The usual manifestations of delayed gastric emptying (e.g., nausea, vomiting, heartburn, persistent fullness after meals, and anorexia) appear to respond to metoclopramide within different time intervals. Significant relief of nausea occurs early and continues to improve over a three-week period. Relief of vomiting and anorexia may precede the relief of abdominal fullness by one week or more.
11-Digit NDC Billing Format:
62559019016
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
473 ML
NDC to RxNorm Crosswalk:
  • RxCUI: 104884 - metoclopramide 5 MG in 5 mL Oral Solution
  • RxCUI: 104884 - metoclopramide 1 MG/ML Oral Solution
  • RxCUI: 104884 - metoclopramide (as the monohydrochloride monohydrate) 5 MG per 5 ML Oral Solution
  • RxCUI: 104884 - metoclopramide 5 MG per 5 ML Oral Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Ani Pharmaceuticals, Inc.
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • METOCLOPRAMIDE HYDROCHLORIDE 5 mg/5mL
    • Pharmacologic Class(es):
  • Dopamine D2 Antagonists - [MoA] (Mechanism of Action)
  • Dopamine-2 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA071402
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    05-18-2015
    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 62559-190-16?

    The NDC Packaged Code 62559-190-16 is assigned to a package of 473 ml in 1 bottle, plastic of Metoclopramide, a human prescription drug labeled by Ani Pharmaceuticals, Inc.. The product's dosage form is solution and is administered via oral form.

    Is NDC 62559-190 included in the NDC Directory?

    Yes, Metoclopramide with product code 62559-190 is active and included in the NDC Directory. The product was first marketed by Ani Pharmaceuticals, Inc. on May 18, 2015 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 62559-190-16?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 473.

    What is the 11-digit format for NDC 62559-190-16?

    The 11-digit format is 62559019016. 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
    5-3-262559-190-165-4-262559-0190-16