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  5. NDC Package Code: 70518-0086-0 Urocit-k

NDC Package 70518-0086-0 Urocit-k

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:
70518-0086-0
Package Description:
30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product Code:
70518-0086
Proprietary Name:
Urocit-k
Usage Information:
This medication is used to make the urine less acidic. This effect helps the kidneys get rid of uric acid, thereby helping to prevent gout and kidney stones. This medication can also prevent and treat certain metabolic problems (acidosis) caused by kidney disease. Citric acid and citrate salts (which contain potassium and sodium) belong to a class of drugs known as urinary alkalinizers. If you have a condition that requires you to limit your intake of potassium and sodium, your doctor may direct you to take a product that is lower in potassium and sodium.
11-Digit NDC Billing Format:
70518008600
Labeler Name:
Remedyrepack Inc.
Sample Package:
No
FDA Application Number:
NDA019071
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
12-27-2016
End Marketing Date:
01-19-2018
Listing Expiration Date:
01-19-2018
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 70518-0086-0?

The NDC Packaged Code 70518-0086-0 is assigned to a package of 30 tablet, extended release in 1 blister pack of Urocit-k, labeled by Remedyrepack Inc.. The product's dosage form is and is administered via form.

Is NDC 70518-0086 included in the NDC Directory?

No, Urocit-k with product code 70518-0086 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Remedyrepack Inc. on December 27, 2016 and its listing in the NDC Directory is set to expire on January 19, 2018 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70518-0086-0?

The 11-digit format is 70518008600. 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
5-4-170518-0086-05-4-270518-0086-00