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  5. NDC Package Code: 0615-7698-39 Metoclopramide

NDC Package 0615-7698-39 Metoclopramide

Tablet 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:
0615-7698-39
Package Description:
30 TABLET in 1 BLISTER PACK
Product Code:
0615-7698
Proprietary Name:
Metoclopramide
Non-Proprietary Name:
Metoclopramide
Substance Name:
Metoclopramide Hydrochloride
Usage Information:
The use of metoclopramide tablets is recommended for adults only. Therapy should not exceed 12 weeks in duration.
11-Digit NDC Billing Format:
00615769839
NDC to RxNorm Crosswalk:
  • RxCUI: 311666 - metoclopramide HCl 10 MG Oral Tablet
  • RxCUI: 311666 - metoclopramide 10 MG Oral Tablet
  • RxCUI: 311666 - metoclopramide (as metoclopramide HCl) 10 MG Oral Tablet
  • RxCUI: 311668 - metoclopramide HCl 5 MG Oral Tablet
  • RxCUI: 311668 - metoclopramide 5 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Ncs Healthcare Of Ky, Llc Dba Vangard Labs
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • METOCLOPRAMIDE HYDROCHLORIDE 5 mg/1
    • Pharmacologic Class(es):
  • Dopamine D2 Antagonists - [MoA] (Mechanism of Action)
  • Dopamine-2 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA072801
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-18-2011
    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 0615-7698-39?

    The NDC Packaged Code 0615-7698-39 is assigned to a package of 30 tablet in 1 blister pack of Metoclopramide, a human prescription drug labeled by Ncs Healthcare Of Ky, Llc Dba Vangard Labs. The product's dosage form is tablet and is administered via oral form.

    Is NDC 0615-7698 included in the NDC Directory?

    Yes, Metoclopramide with product code 0615-7698 is active and included in the NDC Directory. The product was first marketed by Ncs Healthcare Of Ky, Llc Dba Vangard Labs on November 18, 2011 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 0615-7698-39?

    The 11-digit format is 00615769839. 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
    4-4-20615-7698-395-4-200615-7698-39