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  5. NDC Package Code: 68084-419-01 Potassium Chloride

NDC Package 68084-419-01 Potassium Chloride

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 .

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:
68084-419-01
Package Description:
100 BLISTER PACK in 1 CARTON / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68084-419-11)
Product Code:
68084-419
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:
68084041901
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:
American Health Packaging
Sample Package:
No
FDA Application Number:
NDA018238
Marketing Category:
NDA AUTHORIZED GENERIC - A product marketed as a "generic" drug under an approved New Drug Application (NDA), rather than an Abbreviated New Drug Application (ANDA),.
Start Marketing Date:
06-26-2012
End Marketing Date:
08-31-2019
Listing Expiration Date:
08-31-2019
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 68084-419-01?

The NDC Packaged Code 68084-419-01 is assigned to a package of 100 blister pack in 1 carton / 1 capsule, extended release in 1 blister pack (68084-419-11) of Potassium Chloride, labeled by American Health Packaging. The product's dosage form is and is administered via form.

Is NDC 68084-419 included in the NDC Directory?

The product was first marketed by American Health Packaging on June 26, 2012 and its listing in the NDC Directory is set to expire on August 31, 2019 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 68084-419-01?

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 68084-419-01?

The 11-digit format is 68084041901. 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
5-3-268084-419-015-4-268084-0419-01