tylenol extra strength

Generic: acetaminophen

Labeler: navajo manufacturing company inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name tylenol extra strength
Generic Name acetaminophen
Labeler navajo manufacturing company inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Navajo Manufacturing Company Inc.

Identifiers & Regulatory

Product NDC 67751-167
Product ID 67751-167_2385e645-881c-5dd8-e063-6394a90adfab
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2016-09-22

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67751167
Hyphenated Format 67751-167

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
  • 1 POUCH in 1 CARTON (67751-167-01) / 2 TABLET, FILM COATED in 1 POUCH
  • 1 POUCH in 1 CARTON (67751-167-02) / 4 TABLET, FILM COATED in 1 POUCH
  • 12 POUCH in 1 TRAY (67751-167-04) / 1 TABLET, FILM COATED in 1 POUCH
source: ndc

Packages (3)

67751-167-01 1 POUCH in 1 CARTON (67751-167-01) / 2 TABLET, FILM COATED in 1 POUCH 67751-167-02 1 POUCH in 1 CARTON (67751-167-02) / 4 TABLET, FILM COATED in 1 POUCH 67751-167-04 12 POUCH in 1 TRAY (67751-167-04) / 1 TABLET, FILM COATED in 1 POUCH

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (2)

Tylenol Extra Strength ndc-match (0.9) Tylenol Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2385e645-881c-5dd8-e063-6394a90adfab", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440", "209459"], "spl_set_id": ["86b6ac01-3866-4cd8-a1be-9babb6ff311b"], "manufacturer_name": ["Navajo Manufacturing Company Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (67751-167-01)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "67751-167-01", "marketing_start_date": "20160922"}, {"sample": false, "description": "1 POUCH in 1 CARTON (67751-167-02)  / 4 TABLET, FILM COATED in 1 POUCH", "package_ndc": "67751-167-02", "marketing_start_date": "20160922"}, {"sample": false, "description": "12 POUCH in 1 TRAY (67751-167-04)  / 1 TABLET, FILM COATED in 1 POUCH", "package_ndc": "67751-167-04", "marketing_end_date": "20260331", "marketing_start_date": "20160922"}], "brand_name": "Tylenol Extra Strength", "product_id": "67751-167_2385e645-881c-5dd8-e063-6394a90adfab", "dosage_form": "TABLET, FILM COATED", "product_ndc": "67751-167", "generic_name": "ACETAMINOPHEN", "labeler_name": "Navajo Manufacturing Company Inc.", "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": "20160922", "listing_expiration_date": "20261231"}