Butalbital, Acetaminophen And Caffeine
NDC Package 46672-059-10

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Butalbital, Acetaminophen And Caffeine is a . Marketed by Mikart, Inc., this product is identified by NDC 46672-059 and is authorized under FDA application ANDA089451.

Identification & Billing

NDC Package Code
46672-059-10
Package Description
100 TABLET in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
46672005910

Clinical Specifications

Proprietary Name
Butalbital, Acetaminophen And Caffeine
Dosage Form
-

Regulatory & Marketing

Labeler Name
Mikart, Inc.
FDA Application #
ANDA089451
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
05-23-1988
End Marketing Date
01-14-2014
Listing Expiration
01-14-2014
Exclude Flag
D
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (46672-059). Click a package code to view its specific billing and regulatory data.

500 TABLET in 1 BOTTLE, PLASTIC

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 46672-059-10 identifies a specific commercial package of 100 tablet in 1 bottle, plastic of Butalbital, Acetaminophen And Caffeine, labeled by Mikart, Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Mikart, Inc. on May 23, 1988. The current certification is valid through January 14, 2014.

How is this Mikart, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 46672005910. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
46672-059-10
11-Digit CMS (5-4-2)
46672-0059-10

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.