Package 50580-491-70

Brand: tylenol extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 50580-491-70
Digits Only 5058049170
Product NDC 50580-491
Description

1 BOTTLE in 1 CARTON (50580-491-70) / 700 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-08-30
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": "4961695d-72f4-533a-e063-6294a90a5a29", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440", "209459"], "spl_set_id": ["4961695d-72f3-533a-e063-6294a90a5a29"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-491-01)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-491-01", "marketing_start_date": "20250830"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (50580-491-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50580-491-10", "marketing_start_date": "20250830"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-491-70)  / 700 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-491-70", "marketing_start_date": "20250830"}], "brand_name": "TYLENOL Extra Strength", "product_id": "50580-491_4961695d-72f4-533a-e063-6294a90a5a29", "dosage_form": "TABLET, FILM COATED", "product_ndc": "50580-491", "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": "20250830", "listing_expiration_date": "20271231"}