NDC Package 0186-4010-02 Nexium

Esomeprazole Magnesium Granule, Delayed Release Oral - View Billable Units, 11-Digit Format, RxNorm

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:
0186-4010-02
Package Description:
5 GRANULE, DELAYED RELEASE in 1 CARTON
Product Code:
Proprietary Name:
Nexium
Non-Proprietary Name:
Esomeprazole Magnesium
Substance Name:
Esomeprazole Magnesium
Usage Information:
Esomeprazole is used to treat certain stomach and esophagus problems (such as acid reflux, ulcers). It works by decreasing the amount of acid your stomach makes. It relieves symptoms such as heartburn, difficulty swallowing, and persistent cough. This medication helps heal acid damage to the stomach and esophagus, helps prevent ulcers, and may help prevent cancer of the esophagus. Esomeprazole belongs to a class of drugs known as proton pump inhibitors (PPIs).
11-Digit NDC Billing Format:
00186401002
NDC to RxNorm Crosswalk:
  • RxCUI: 1297658 - esomeprazole 2.5 MG Granules for Delayed Release Oral Suspension
  • RxCUI: 1297658 - esomeprazole 2.5 MG Granules for Oral Suspension
  • RxCUI: 1297658 - esomeprazole (as esomeprazole magnesium) 2.5 MG Granules for Delayed Release Oral Suspension
  • RxCUI: 1297660 - NexIUM 2.5 MG Granules for Delayed Release Oral Suspension
  • RxCUI: 1297660 - esomeprazole 2.5 MG Granules for Oral Suspension [Nexium]
Product Type:
Human Prescription Drug
Labeler Name:
Astrazeneca Pharmaceuticals Lp
Dosage Form:
Granule, Delayed Release - A small medicinal particle or grain to which an enteric or other coating has been applied, thus delaying release of the drug until its passage into the intestines.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Sample Package:
Yes
FDA Application Number:
NDA022101
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
07-07-2008
Listing Expiration Date:
12-31-2025
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.

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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
0186-4010-0130 GRANULE, DELAYED RELEASE in 1 CARTON

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Frequently Asked Questions

What is NDC 0186-4010-02?

The NDC Packaged Code 0186-4010-02 is assigned to a package of 5 granule, delayed release in 1 carton of Nexium, a human prescription drug labeled by Astrazeneca Pharmaceuticals Lp. The product's dosage form is granule, delayed release and is administered via oral form.

Is NDC 0186-4010 included in the NDC Directory?

Yes, Nexium with product code 0186-4010 is active and included in the NDC Directory. The product was first marketed by Astrazeneca Pharmaceuticals Lp on July 07, 2008 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0186-4010-02?

The 11-digit format is 00186401002. 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
4-4-20186-4010-025-4-200186-4010-02