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  5. NDC Package Code: 68001-235-08 Potassium Chloride

NDC Package 68001-235-08 Potassium Chloride

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
68001-235-08
Package Description:
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Code:
68001-235
Proprietary Name:
Potassium Chloride
Usage Information:
This medication is a mineral supplement used to treat or prevent low amounts of potassium in the blood. A normal level of potassium in the blood is important. Potassium helps your cells, kidneys, heart, muscles, and nerves work properly. Most people get enough potassium by eating a well-balanced diet. Some conditions that can lower your body's potassium level include severe prolonged diarrhea and vomiting, hormone problems such as hyperaldosteronism, or treatment with "water pills"/diuretics.
11-Digit NDC Billing Format:
68001023508
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1000 EA
Labeler Name:
Bluepoint Laboratories
Sample Package:
No
FDA Application Number:
ANDA076368
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
02-25-2014
End Marketing Date:
11-30-2022
Listing Expiration Date:
11-30-2022
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
68001-235-00100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
68001-235-03500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 68001-235-08?

The NDC Packaged Code 68001-235-08 is assigned to a package of 1000 tablet, extended release in 1 bottle, plastic of Potassium Chloride, labeled by Bluepoint Laboratories. The product's dosage form is and is administered via form.

Is NDC 68001-235 included in the NDC Directory?

No, Potassium Chloride with product code 68001-235 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Bluepoint Laboratories on February 25, 2014 and its listing in the NDC Directory is set to expire on November 30, 2022 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 68001-235-08?

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 1000.

What is the 11-digit format for NDC 68001-235-08?

The 11-digit format is 68001023508. 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
5-3-268001-235-085-4-268001-0235-08