Acetaminophen, Aspirin, And Caffeine Tablet, Coated
NDC Package 68210-1013-0

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

Acetaminophen, Aspirin, And Caffeine tablets is a drug for further processing. This formulation utilizes a tablet, coated delivery system. Marketed by Prodose, Inc., this product is identified by NDC 68210-1013.

Identification & Billing

NDC Package Code
68210-1013-0
Package Description
1 BAG in 1 DRUM / 30000 TABLET, COATED in 1 BAG
Product Code
68210-1013
11-Digit Billing Format
68210101300

Clinical Specifications

Proprietary Name
Acetaminophen, Aspirin, And Caffeine
Non-Proprietary Name
Acetaminophen, Aspirin, And Caffeine
Substance Name
Acetaminophen; Aspirin; Caffeine
Dosage Form
Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
Active Ingredient(s)

Regulatory & Marketing

Labeler Name
Prodose, Inc.
Product Type
Drug For Further Processing
Marketing Category
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date
06-19-2015
Listing Expiration
12-31-2027
Exclude Flag
N
Unfinished Product
Yes
Sample Package
N/A

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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 68210-1013-0 identifies a specific commercial package of 1 bag in 1 drum / 30000 tablet, coated in 1 bag of Acetaminophen, Aspirin, And Caffeine (UNFINISHED drug), drug for further processing labeled by Prodose, Inc.. This tablet, coated is formulated for use and contains acetaminophen; aspirin; caffeine as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Prodose, Inc. on June 19, 2015. The current certification is valid through December 31, 2027.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68210101300. 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 (5-4-1)
68210-1013-0
11-Digit CMS (5-4-2)
68210-1013-00

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