NDC Package 70771-1023-5 Pioglitazone

View Billable Units, 11-Digit Format, RxNorm

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:
70771-1023-5
Package Description:
500 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Pioglitazone
Usage Information:
Monotherapy and Combination TherapyPioglitazone tablets, USP are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus in multiple clinical settings [see Clinical Studies (14)].Important Limitations of UsePioglitazone hydrochloride exerts its antihyperglycemic effect only in the presence of endogenous insulin. Pioglitazone hydrochloride should not be used to treat type 1 diabetes or diabetic ketoacidosis, as it would not be effective in these settings.Use caution in patients with liver disease [see Warnings and Precautions (5.3)].
11-Digit NDC Billing Format:
70771102305
Labeler Name:
Zydus Lifesciences Limited
Sample Package:
No
FDA Application Number:
ANDA202456
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
11-16-2016
End Marketing Date:
05-08-2025
Listing Expiration Date:
05-08-2025
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.

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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
70771-1023-01000 TABLET in 1 BOTTLE
70771-1023-1100 TABLET in 1 BOTTLE
70771-1023-330 TABLET in 1 BOTTLE
70771-1023-410 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
70771-1023-990 TABLET in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 70771-1023-5?

The NDC Packaged Code 70771-1023-5 is assigned to a package of 500 tablet in 1 bottle of Pioglitazone, labeled by Zydus Lifesciences Limited. The product's dosage form is and is administered via form.

Is NDC 70771-1023 included in the NDC Directory?

No, Pioglitazone with product code 70771-1023 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Zydus Lifesciences Limited on November 16, 2016 and its listing in the NDC Directory is set to expire on May 08, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70771-1023-5?

The 11-digit format is 70771102305. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
5-4-170771-1023-55-4-270771-1023-05