panadol extra strength

Generic: acetaminophen

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

Drug Facts

Product Profile

Brand Name panadol extra strength
Generic Name acetaminophen
Labeler haleon us holdings llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0135-0609
Product ID 0135-0609_10c10ae1-2b66-f708-e063-6394a90a0fca
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2017-03-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01350609
Hyphenated Format 0135-0609

Supplemental Identifiers

RxCUI
198440 200977
UNII
362O9ITL9D

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 panadol extra strength (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0135-0609-01) / 24 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0135-0609-02) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0135-0609-03) / 100 TABLET, FILM COATED in 1 BOTTLE
  • 50 PACKET in 1 CARTON (0135-0609-04) / 2 TABLET, FILM COATED in 1 PACKET (0135-0609-05)
source: ndc

Packages (4)

0135-0609-01 1 BOTTLE in 1 CARTON (0135-0609-01) / 24 TABLET, FILM COATED in 1 BOTTLE 0135-0609-02 1 BOTTLE in 1 CARTON (0135-0609-02) / 50 TABLET, FILM COATED in 1 BOTTLE 0135-0609-03 1 BOTTLE in 1 CARTON (0135-0609-03) / 100 TABLET, FILM COATED in 1 BOTTLE 0135-0609-04 50 PACKET in 1 CARTON (0135-0609-04) / 2 TABLET, FILM COATED in 1 PACKET (0135-0609-05)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

PANADOL Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "10c10ae1-2b66-f708-e063-6394a90a0fca", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440", "200977"], "spl_set_id": ["b2fe7f47-1a2e-40ee-8f8f-38f2028dce1b"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0135-0609-01)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0135-0609-01", "marketing_start_date": "20170315"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0135-0609-02)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0135-0609-02", "marketing_start_date": "20170315"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0135-0609-03)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0135-0609-03", "marketing_start_date": "20170315"}, {"sample": false, "description": "50 PACKET in 1 CARTON (0135-0609-04)  / 2 TABLET, FILM COATED in 1 PACKET (0135-0609-05)", "package_ndc": "0135-0609-04", "marketing_start_date": "20170315"}], "brand_name": "PANADOL Extra Strength", "product_id": "0135-0609_10c10ae1-2b66-f708-e063-6394a90a0fca", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0135-0609", "generic_name": "acetaminophen", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PANADOL", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170315", "listing_expiration_date": "20261231"}