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  5. NDC Package Code: 71930-010-10 Alosetron Hydrochloride

NDC Package 71930-010-10 Alosetron Hydrochloride

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:
71930-010-10
Package Description:
30 TABLET in 1 BOTTLE
Product Code:
71930-010
Proprietary Name:
Alosetron Hydrochloride
Non-Proprietary Name:
Alosetron Hydrochloride
Substance Name:
Alosetron Hydrochloride
Usage Information:
Alosetron tablets are indicated only for women with severe diarrhea-predominant irritable bowel syndrome (IBS) who have:chronic IBS symptoms (generally lasting 6 months or longer), had anatomic or biochemical abnormalities of the gastrointestinal tract excluded, and not responded adequately to conventional therapy. Diarrhea-predominant IBS is severe if it includes diarrhea and one or more of the following: frequent and severe abdominal pain/discomfort, frequent bowel urgency or fecal incontinence, disability or restriction of daily activities due to IBS. Because of infrequent but serious gastrointestinal adverse reactions associated with alosetron tablets, the indication is restricted to those patients for whom the benefit-to-risk balance is most favorable. Clinical studies have not been performed to adequately confirm the benefits of alosetron tablets in men.
11-Digit NDC Billing Format:
71930001010
Product Type:
Human Prescription Drug
Labeler Name:
Eywa Pharma Inc
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):
ALOSETRON HYDROCHLORIDE .5 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA211621
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
08-01-2025
Listing Expiration Date:
12-31-2026
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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Frequently Asked Questions

What is NDC 71930-010-10?

The NDC Packaged Code 71930-010-10 is assigned to a package of 30 tablet in 1 bottle of Alosetron Hydrochloride, a human prescription drug labeled by Eywa Pharma Inc. The product's dosage form is tablet and is administered via oral form.

Is NDC 71930-010 included in the NDC Directory?

Yes, Alosetron Hydrochloride with product code 71930-010 is active and included in the NDC Directory. The product was first marketed by Eywa Pharma Inc on August 01, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 71930-010-10?

The 11-digit format is 71930001010. 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
5-3-271930-010-105-4-271930-0010-10