acetaminophen extra strength

Generic: acetaminophen

Labeler: fsa store inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen extra strength
Generic Name acetaminophen
Labeler fsa store inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
FSA Store Inc.

Identifiers & Regulatory

Product NDC 81522-104
Product ID 81522-104_24996677-f6f7-01be-e063-6394a90a10d7
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2023-01-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 81522104
Hyphenated Format 81522-104

Supplemental Identifiers

RxCUI
198440
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 acetaminophen 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, PLASTIC in 1 CARTON (81522-104-04) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 500 TABLET, COATED in 1 BOTTLE, PLASTIC (81522-104-06)
source: ndc

Packages (2)

81522-104-04 1 BOTTLE, PLASTIC in 1 CARTON (81522-104-04) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC 81522-104-06 500 TABLET, COATED in 1 BOTTLE, PLASTIC (81522-104-06)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Acetaminophen Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "24996677-f6f7-01be-e063-6394a90a10d7", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["ec6add55-f4a3-7818-e053-2a95a90aee04"], "manufacturer_name": ["FSA Store Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (81522-104-04)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "81522-104-04", "marketing_start_date": "20230111"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE, PLASTIC (81522-104-06)", "package_ndc": "81522-104-06", "marketing_start_date": "20230503"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "81522-104_24996677-f6f7-01be-e063-6394a90a10d7", "dosage_form": "TABLET, COATED", "product_ndc": "81522-104", "generic_name": "Acetaminophen", "labeler_name": "FSA Store Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230111", "listing_expiration_date": "20261231"}