NDC Package 70710-1072-3 Modafinil

View Billable Units, 11-Digit Format, RxNorm

Package Information
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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:

70710-1072-3

Package Description:

30 TABLET in 1 BOTTLE

Product Code:

70710-1072

Proprietary Name:

Modafinil

Usage Information:

Modafinil reduces extreme sleepiness due to narcolepsy and other sleep disorders, such as periods of stopped breathing during sleep (obstructive sleep apnea). It is also used to help you stay awake during work hours if you have a work schedule that keeps you from having a normal sleep routine (shift work sleep disorder). This medication does not cure these sleep disorders and may not get rid of all your sleepiness. Modafinil does not take the place of getting enough sleep. It should not be used to treat tiredness or hold off sleep in people who do not have a sleep disorder. It is not known how modafinil works to keep you awake. It is thought to work by affecting certain substances in the brain that control the sleep/wake cycle.

11-Digit NDC Billing Format:

70710107203

Labeler Name:

Zydus Pharmaceuticals Usa Inc.

Sample Package:

FDA Application Number:

ANDA209966

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

01-04-2018

End Marketing Date:

07-09-2022

Listing Expiration Date:

07-09-2022

Exclude Flag:

Code Structure:

70710 - Zydus Pharmaceuticals Usa Inc.
- 70710-1072 - Modafinil
  - 70710-1072-3 - 30 TABLET in 1 BOTTLE

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 Code	Package Description
70710-1072-1	100 TABLET in 1 BOTTLE
70710-1072-9	90 TABLET in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 70710-1072-3?

The NDC Packaged Code 70710-1072-3 is assigned to a package of 30 tablet in 1 bottle of Modafinil, labeled by Zydus Pharmaceuticals Usa Inc.. The product's dosage form is and is administered via form.

Is NDC 70710-1072 included in the NDC Directory?

No, Modafinil with product code 70710-1072 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Zydus Pharmaceuticals Usa Inc. on January 04, 2018 and its listing in the NDC Directory is set to expire on July 09, 2022 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70710-1072-3?

The 11-digit format is 70710107203. 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 5-4-1 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-4-1	70710-1072-3	5-4-2	70710-1072-03

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