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  4. NDC Product Code: 50436-0576 Metoclopramide

NDC 50436-0576 Metoclopramide

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 50436-0576?
  5. Metoclopramide Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50436-0576
Proprietary Name:
Metoclopramide
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Unit Dose Services
Labeler Code:
50436
Product Label ID:
cf6a64e0-98ac-46a6-8d2a-1dd963cc65c5
Start Marketing Date: [9]
06-01-1991
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)
Flavor(s):
BERRY (C73365 - BERRY CITRIS)

Product Packages

NDC Code 50436-0576-1

Package Description: 1 mL in 1 SYRINGE, PLASTIC

Product Details

What is NDC 50436-0576?

The NDC code 50436-0576 is assigned by the FDA to the product Metoclopramide which is product labeled by Unit Dose Services. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50436-0576-1 1 ml in 1 syringe, plastic . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Metoclopramide?

The use of Metoclopramide Oral Solution is recommended for adults only. Therapy should not exceed 12 weeks in duration.

Which are Metoclopramide UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Metoclopramide Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Metoclopramide?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • 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

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".