Package 67751-167-03

Brand: tylenol extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 67751-167-03
Digits Only 6775116703
Product NDC 67751-167
Product ID 67751-167_f6f71bb0-5b9b-59f7-e053-6394a90abf8e
Description

2 TRAY in 1 POUCH (67751-167-03) / 12 TABLET, FILM COATED in 1 TRAY

Marketing

Marketing Status
Discontinued 2026-03-31
Brand tylenol extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Tylenol Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f6f71bb0-5b9b-59f7-e053-6394a90abf8e", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440", "209459"], "spl_set_id": ["65bf1556-f25a-9439-e053-2a91aa0a3194"], "manufacturer_name": ["Navajo Manufacturing Company Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2 TRAY in 1 POUCH (67751-167-03)  / 12 TABLET, FILM COATED in 1 TRAY", "package_ndc": "67751-167-03", "marketing_end_date": "20260331", "marketing_start_date": "20171204"}], "brand_name": "Tylenol Extra Strength", "product_id": "67751-167_f6f71bb0-5b9b-59f7-e053-6394a90abf8e", "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": "20171204", "listing_expiration_date": "20261231"}