tylenol extra strength

Generic: acetaminophen

Labeler: morning star otc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name tylenol extra strength
Generic Name acetaminophen
Labeler morning star otc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Morning Star OTC

Identifiers & Regulatory

Product NDC 53209-1001
Product ID 53209-1001_37e8d749-91bb-a5bc-e063-6394a90ac8a8
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 1984-08-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 532091001
Hyphenated Format 53209-1001

Supplemental Identifiers

RxCUI
198440 209459
UNII
362O9ITL9D

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 tylenol 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
  • 25 BLISTER PACK in 1 POUCH (53209-1001-2) / 2 TABLET, FILM COATED in 1 BLISTER PACK (53209-1001-1)
source: ndc

Packages (1)

53209-1001-2 25 BLISTER PACK in 1 POUCH (53209-1001-2) / 2 TABLET, FILM COATED in 1 BLISTER PACK (53209-1001-1)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

TYLENOL Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "37e8d749-91bb-a5bc-e063-6394a90ac8a8", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440", "209459"], "spl_set_id": ["8502ea21-937d-4b33-a3e0-ffab5dc38cd8"], "manufacturer_name": ["Morning Star OTC"]}, "finished": true, "packaging": [{"sample": false, "description": "25 BLISTER PACK in 1 POUCH (53209-1001-2)  / 2 TABLET, FILM COATED in 1 BLISTER PACK (53209-1001-1)", "package_ndc": "53209-1001-2", "marketing_start_date": "20250619"}], "brand_name": "TYLENOL Extra Strength", "product_id": "53209-1001_37e8d749-91bb-a5bc-e063-6394a90ac8a8", "dosage_form": "TABLET, FILM COATED", "product_ndc": "53209-1001", "generic_name": "Acetaminophen", "labeler_name": "Morning Star OTC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TYLENOL Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19840819", "listing_expiration_date": "20261231"}