Excedrin Tablet, Film Coated
NDC Package 0067-2000-33

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

Package Information

Excedrin (acetaminophen, aspirin (nsaid), and caffeine) tablets is •do not use more than directed•adults and children 12 years and over: take 2 caplets every 6 hours; not more than 6 caplets in 24 hours•children under 12 years: ask a doctor •do not use more than directed•drink a full glass of water with each dose•adults and children 12 years and over: take 2 caplets every 6 hours; not more than 8 caplets in 24 hours•children under 12 years: ask a doctor. This formulation utilizes a tablet, film coated delivery system. Marketed by Haleon Us Holdings Llc, this product is identified by NDC 0067-2000 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
0067-2000-33
Package Description
1 BOTTLE in 1 CARTON / 300 TABLET, FILM COATED in 1 BOTTLE
Product Code
0067-2000
11-Digit Billing Format
00067200033
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
1 EA
RxNorm Crosswalk
  • RxCUI: 209468 - EXCEDRIN 250 MG / 250 MG / 65 MG Oral Tablet
  • RxCUI: 209468 - acetaminophen 250 MG / aspirin 250 MG / caffeine 65 MG Oral Tablet [Excedrin]
  • RxCUI: 209468 - APAP 250 MG / ASA 250 MG / Caffeine 65 MG Oral Tablet [Excedrin]
  • RxCUI: 209468 - Excedrin Extra Strength (APAP 250 MG / ASA 250 MG / caffeine 65 MG) Oral Tablet
  • RxCUI: 209468 - Excedrin Menstrual Complete (APAP 250 MG / ASA 250 MG / caffeine 65 MG) Oral Tablet

Clinical Specifications

Proprietary Name
Excedrin Extra Strength Pain Reliever
Non-Proprietary Name
Acetaminophen, Aspirin (nsaid), And Caffeine
Substance Name
Acetaminophen; Aspirin; Caffeine
Dosage Form
Tablet, Film Coated - 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.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
•do not use more than directed•adults and children 12 years and over: take 2 caplets every 6 hours; not more than 6 caplets in 24 hours•children under 12 years: ask a doctor •do not use more than directed•drink a full glass of water with each dose•adults and children 12 years and over: take 2 caplets every 6 hours; not more than 8 caplets in 24 hours•children under 12 years: ask a doctor

Regulatory & Marketing

Labeler Name
Haleon Us Holdings Llc
Product Type
Human Otc Drug
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-27-2006
Listing Expiration
12-31-2026
Exclude Flag
N
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 (0067-2000). Click a package code to view its specific billing and regulatory data.

0067-2000-02
2 TABLET, FILM COATED in 1 POUCH
0067-2000-07
250 TABLET, FILM COATED in 1 BOTTLE
0067-2000-10
1 BOTTLE in 1 CARTON / 10 TABLET, FILM COATED in 1 BOTTLE
0067-2000-20
1 BOTTLE in 1 CARTON / 200 TABLET, FILM COATED in 1 BOTTLE
0067-2000-24
1 BOTTLE in 1 CARTON / 24 TABLET, FILM COATED in 1 BOTTLE
0067-2000-30
1 BOTTLE in 1 CARTON / 30 TABLET, FILM COATED in 1 BOTTLE
0067-2000-50
1 BOTTLE in 1 CARTON / 50 TABLET, FILM COATED in 1 BOTTLE
0067-2000-77
1 BOTTLE in 1 CARTON / 250 TABLET, FILM COATED in 1 BOTTLE
0067-2000-83
1 BOTTLE in 1 CARTON / 125 TABLET, FILM COATED in 1 BOTTLE
0067-2000-91
1 BOTTLE in 1 CARTON / 100 TABLET, FILM COATED in 1 BOTTLE
0067-2000-94
100 TABLET, FILM COATED in 1 BOTTLE

* 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 0067-2000-33 identifies a specific commercial package of 1 bottle in 1 carton / 300 tablet, film coated in 1 bottle of Excedrin Extra Strength Pain Reliever, a human over the counter drug labeled by Haleon Us Holdings Llc. This tablet, film coated is formulated for oral 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 Haleon Us Holdings Llc on September 27, 2006. The current certification is valid through December 31, 2026.

How is this Haleon Us Holdings Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00067200033. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 1 total billable units per package. 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 (4-4-2)
0067-2000-33
11-Digit CMS (5-4-2)
00067-2000-33

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