Package 50580-108-25

Brand: tylenol extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 50580-108-25
Digits Only 5058010825
Product NDC 50580-108
Product ID 50580-108_3f653262-b932-7d42-e063-6394a90adddd
Description

1 BOTTLE in 1 CARTON (50580-108-25) / 225 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-10-13
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": "3f653262-b932-7d42-e063-6394a90adddd", "openfda": {"upc": ["0300450444271"], "unii": ["362O9ITL9D"], "rxcui": ["198440", "209459"], "spl_set_id": ["3f653262-b931-7d42-e063-6394a90adddd"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-108-25)  / 225 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-108-25", "marketing_start_date": "20251013"}], "brand_name": "TYLENOL Extra Strength", "product_id": "50580-108_3f653262-b932-7d42-e063-6394a90adddd", "dosage_form": "TABLET, FILM COATED", "product_ndc": "50580-108", "generic_name": "acetaminophen", "labeler_name": "Kenvue Brands LLC", "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": "20251013", "listing_expiration_date": "20261231"}