Package 50580-187-08

Brand: tylenol extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 50580-187-08
Digits Only 5058018708
Product NDC 50580-187
Description

1 BOTTLE in 1 CARTON (50580-187-08) / 240 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-11-28
Brand tylenol extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "423280b2-1f17-3a41-e063-6394a90a61e6", "openfda": {"upc": ["0300450420084"], "unii": ["362O9ITL9D"], "rxcui": ["307668", "828555"], "spl_set_id": ["42321456-d7dd-3b51-e063-6394a90ac292"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-187-08)  / 240 mL in 1 BOTTLE", "package_ndc": "50580-187-08", "marketing_start_date": "20251128"}], "brand_name": "TYLENOL Extra Strength", "product_id": "50580-187_423280b2-1f17-3a41-e063-6394a90a61e6", "dosage_form": "SUSPENSION", "product_ndc": "50580-187", "generic_name": "ACETAMINOPHEN", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TYLENOL Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "960 mg/30mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251128", "listing_expiration_date": "20261231"}