1. Home
  2. Labeler Index
  3. Everlight Chemical Industrial Corporation Kuanyin Ii Plant
  4. 65035-132
  5. NDC Package Code: 65035-132-10 Lubiprostone

NDC Package 65035-132-10 Lubiprostone

Powder - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
65035-132-10
Package Description:
10 g in 1 BOTTLE
Product Code:
65035-132
Non-Proprietary Name:
Lubiprostone
Substance Name:
Lubiprostone
Usage Information:
This medication is used to treat certain types of constipation (chronic idiopathic constipation, irritable bowel syndrome with constipation). Chronic idiopathic constipation has an unknown cause and is not due to diet, other diseases, or drugs. Lubiprostone is also used to treat constipation caused by opioid medications in people with ongoing pain due to medical conditions other than cancer. This medication may improve symptoms such as bloating and abdominal discomfort, improve stool texture, lessen the need to strain, and decrease the feeling of not completely relieving oneself. Lubiprostone belongs to a class of drugs known as chloride channel activators. It works by increasing the amount of fluid within your intestines, making the passage of stool easier.
11-Digit NDC Billing Format:
65035013210
Product Type:
Bulk Ingredient
Labeler Name:
Everlight Chemical Industrial Corporation Kuanyin Ii Plant
Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Active Ingredient(s):
  • LUBIPROSTONE 1 g/g
    • Sample Package:
    N/A
    Marketing Category:
    BULK INGREDIENT - A category specifying that a product is marketed as a bulk ingredient.
    Start Marketing Date:
    12-12-2014
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Unfinished Product:
    Yes
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    65035-132-011 g in 1 BOTTLE
    65035-132-055 g in 1 BOTTLE
    65035-132-2020 g in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 65035-132-10?

    The NDC Packaged Code 65035-132-10 is assigned to an UNFINISHED drug package of 10 g in 1 bottle of Lubiprostone, a bulk ingredient labeled by Everlight Chemical Industrial Corporation Kuanyin Ii Plant. The product's dosage form is powder and is administered via form.

    Is NDC 65035-132 included in the NDC Directory?

    Yes, Lubiprostone is an UNFINISHED PRODUCT with code 65035-132 that is active and included in the NDC Directory. The product was first marketed by Everlight Chemical Industrial Corporation Kuanyin Ii Plant on December 12, 2014 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 65035-132-10?

    The 11-digit format is 65035013210. 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
    5-3-265035-132-105-4-265035-0132-10