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  5. NDC Package Code: 67046-1575-3 Lithium Carbonate

NDC Package 67046-1575-3 Lithium Carbonate

Tablet, Film Coated, Extended Release Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

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:
67046-1575-3
Package Description:
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product Code:
67046-1575
Proprietary Name:
Lithium Carbonate
Non-Proprietary Name:
Lithium Carbonate
Substance 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:
67046157503
Product Type:
Human Prescription Drug
Labeler Name:
Coupler Llc
Dosage Form:
Tablet, Film Coated, Extended Release - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer; the tablet is formulated in such manner as to make the contained medicament available over an extended period of time following ingestion.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
LITHIUM CARBONATE 300 mg/1
Pharmacologic Class(es):
Mood Stabilizer - [EPC] (Established Pharmacologic Class)
Sample Package:
No
FDA Application Number:
ANDA091544
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
09-04-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
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 67046-1575-3?

The NDC Packaged Code 67046-1575-3 is assigned to a package of 30 tablet, film coated, extended release in 1 blister pack of Lithium Carbonate, a human prescription drug labeled by Coupler Llc. The product's dosage form is tablet, film coated, extended release and is administered via oral form.

Is NDC 67046-1575 included in the NDC Directory?

Yes, Lithium Carbonate with product code 67046-1575 is active and included in the NDC Directory. The product was first marketed by Coupler Llc on September 04, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 67046-1575-3?

The 11-digit format is 67046157503. 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
5-4-167046-1575-35-4-267046-1575-03