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  5. NDC Package Code: 63739-265-10 Lithium Carbonate

NDC Package 63739-265-10 Lithium Carbonate

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:
63739-265-10
Package Description:
10 BLISTER PACK in 1 BOX, UNIT-DOSE / 10 CAPSULE in 1 BLISTER PACK
Product Code:
63739-265
Proprietary Name:
Lithium Carbonate
Usage Information:
This medication is used to treat manic-depressive disorder (bipolar disorder). It works to stabilize the mood and reduce extremes in behavior by restoring the balance of certain natural substances (neurotransmitters) in the brain. Some of the benefits of continued use of this medication include decreasing how often manic episodes occur and decreasing the symptoms of manic episodes, such as exaggerated feelings of well-being, feelings that others wish to harm you, irritability, anxiousness, rapid/loud speech, and aggressive/hostile behaviors.
11-Digit NDC Billing Format:
63739026510
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
10 EA
Labeler Name:
Mckesson Corporation
Sample Package:
No
FDA Application Number:
ANDA076243
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
07-19-2007
End Marketing Date:
10-31-2016
Listing Expiration Date:
10-31-2016
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 63739-265-10?

The NDC Packaged Code 63739-265-10 is assigned to a package of 10 blister pack in 1 box, unit-dose / 10 capsule in 1 blister pack of Lithium Carbonate, labeled by Mckesson Corporation. The product's dosage form is and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 10 billable units per package.

Is NDC 63739-265 included in the NDC Directory?

No, Lithium Carbonate with product code 63739-265 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Mckesson Corporation on July 19, 2007 and its listing in the NDC Directory is set to expire on October 31, 2016 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 63739-265-10?

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 10.

What is the 11-digit format for NDC 63739-265-10?

The 11-digit format is 63739026510. 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
5-3-263739-265-105-4-263739-0265-10