excedrin extra strength and excedrin tension headache

Generic: acetaminophen, aspirin (nsaid), and caffeine

Labeler: haleon us holdings llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name excedrin extra strength and excedrin tension headache
Generic Name acetaminophen, aspirin (nsaid), and caffeine
Labeler haleon us holdings llc
Dosage Form KIT
Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0067-8151
Product ID 0067-8151_4b80ea7d-b5ef-e06c-e063-6294a90aafac
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2027-12-31
Marketing Start 2018-09-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00678151
Hyphenated Format 0067-8151

Supplemental Identifiers

RxCUI
209468 307686 308297 404172

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name excedrin extra strength and excedrin tension headache (source: ndc)
Generic Name acetaminophen, aspirin (nsaid), and caffeine (source: ndc)
Application Number M013 (source: ndc)

Resolved Composition

Strengths
  • 500 mg
  • 65 mg
  • 250 mg
source: label
Packaging
  • 1 KIT in 1 PACKAGE, COMBINATION (0067-8151-01) * 1 BOTTLE in 1 CARTON (0067-8139-01) / 24 TABLET, FILM COATED in 1 BOTTLE * 1 BOTTLE in 1 CARTON (0067-2000-91) / 100 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (1)

0067-8151-01 1 KIT in 1 PACKAGE, COMBINATION (0067-8151-01) * 1 BOTTLE in 1 CARTON (0067-8139-01) / 24 TABLET, FILM COATED in 1 BOTTLE * 1 BOTTLE in 1 CARTON (0067-2000-91) / 100 TABLET, FILM COATED in 1 BOTTLE

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Excedrin Extra Strength and Excedrin Tension Headache ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "4b80ea7d-b5ef-e06c-e063-6294a90aafac", "openfda": {"rxcui": ["209468", "307686", "308297", "404172"], "spl_set_id": ["2c8df1c7-7864-48df-939c-d9ae22e0f52c"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE, COMBINATION (0067-8151-01)  *  1 BOTTLE in 1 CARTON (0067-8139-01)  / 24 TABLET, FILM COATED in 1 BOTTLE *  1 BOTTLE in 1 CARTON (0067-2000-91)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0067-8151-01", "marketing_start_date": "20180930"}], "brand_name": "Excedrin Extra Strength and Excedrin Tension Headache", "product_id": "0067-8151_4b80ea7d-b5ef-e06c-e063-6294a90aafac", "dosage_form": "KIT", "product_ndc": "0067-8151", "generic_name": "Acetaminophen, Aspirin (NSAID), and Caffeine", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Excedrin Extra Strength and Excedrin Tension Headache", "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180930", "listing_expiration_date": "20271231"}