Package 50580-590-05
Brand: tylenol extra strength
Generic: acetaminophenPackage Facts
Identity
Package NDC
50580-590-05
Digits Only
5058059005
Product NDC
50580-590
Description
1 BOTTLE in 1 CARTON (50580-590-05) / 100 TABLET, FILM COATED in 1 BOTTLE
Marketing
Marketing Status
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": "22d94fd9-9488-a812-e063-6394a90a7ffc", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440", "209459"], "spl_set_id": ["015a6179-bacb-452d-b594-4de628ddc11d"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-590-04) / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-590-04", "marketing_start_date": "20200731"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-590-05) / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-590-05", "marketing_start_date": "20200731"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-590-06) / 225 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-590-06", "marketing_start_date": "20200731"}], "brand_name": "TYLENOL Extra Strength", "product_id": "50580-590_22d94fd9-9488-a812-e063-6394a90a7ffc", "dosage_form": "TABLET, FILM COATED", "product_ndc": "50580-590", "generic_name": "acetaminophen", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TYLENOL", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180716", "listing_expiration_date": "20261231"}