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  4. NDC Product Code: 40032-580 Metoclopramide Hydrochloride

NDC 40032-580 Metoclopramide Hydrochloride

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 40032-580?
  5. Metoclopramide Hydrochloride 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:
40032-580
Proprietary Name:
Metoclopramide Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Novel Laboratories, Inc.
Labeler Code:
40032
Product Label ID:
3fb9a45e-48ba-45c5-86a7-03a8744888f6
Start Marketing Date: [9]
08-15-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - OFF-WHITE)
Shape:
ROUND (C48348)
Size(s):
12 MM
Imprint(s):
N;580
Score:
1

Product Packages

NDC Code 40032-580-31

Package Description: 10 BLISTER PACK in 1 CARTON / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

Product Details

What is NDC 40032-580?

The NDC code 40032-580 is assigned by the FDA to the product Metoclopramide Hydrochloride which is product labeled by Novel Laboratories, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 40032-580-31 10 blister pack in 1 carton / 10 tablet, orally disintegrating in 1 blister pack. 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 Hydrochloride?

Metoclopramide Hydrochloride Orally Disintegrating Tablets are indicated as short-term (4 to 12 weeks) therapy for adults with symptomatic, documented gastroesophageal reflux disease (GERD) who fail to respond to conventional therapy.

Which are Metoclopramide Hydrochloride UNII Codes?

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

Which are Metoclopramide Hydrochloride 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 Hydrochloride?

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: 608623 - metoclopramide HCl 10 MG Disintegrating Oral Tablet
  • RxCUI: 608623 - metoclopramide 10 MG Disintegrating Oral Tablet
  • RxCUI: 608623 - metoclopramide 10 MG (metoclopramide hydrochloride 11.82 MG) Disintegrating Oral Tablet
  • RxCUI: 608624 - metoclopramide HCl 5 MG Disintegrating Oral Tablet
  • RxCUI: 608624 - metoclopramide 5 MG Disintegrating Oral Tablet

* 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".