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  5. NDC Package Code: 57664-685-88 Miglitol

NDC Package 57664-685-88 Miglitol

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
57664-685-88
Package Description:
100 TABLET, COATED in 1 BOTTLE
Product Code:
57664-685
Proprietary Name:
Miglitol
Usage Information:
Miglitol is used with a proper diet and exercise program to control high blood sugar in people with type 2 diabetes. Controlling high blood sugar helps prevent kidney damage, blindness, nerve problems, loss of limbs, and sexual function problems. Proper control of diabetes may also lessen your risk of a heart attack or stroke. Miglitol works in your intestines to slow the breakdown and absorption of carbohydrates from foods that you eat. This effect helps lessen your blood sugar rise after a meal.
11-Digit NDC Billing Format:
57664068588
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 EA
Labeler Name:
Sun Pharmaceutical Industries Ltd.
Sample Package:
No
FDA Application Number:
ANDA203965
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
01-04-2016
End Marketing Date:
05-31-2023
Listing Expiration Date:
05-31-2023
Exclude Flag:
D
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.

Frequently Asked Questions

What is NDC 57664-685-88?

The NDC Packaged Code 57664-685-88 is assigned to a package of 100 tablet, coated in 1 bottle of Miglitol, labeled by Sun Pharmaceutical Industries Ltd.. The product's dosage form is and is administered via form.

Is NDC 57664-685 included in the NDC Directory?

No, Miglitol with product code 57664-685 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Sun Pharmaceutical Industries Ltd. on January 04, 2016 and its listing in the NDC Directory is set to expire on May 31, 2023 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 57664-685-88?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 100.

What is the 11-digit format for NDC 57664-685-88?

The 11-digit format is 57664068588. 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
5-3-257664-685-885-4-257664-0685-88