Package 50580-472-01
Brand: tylenol extra strength
Generic: acetaminophenPackage Facts
Identity
Package NDC
50580-472-01
Digits Only
5058047201
Product NDC
50580-472
Description
1 BOTTLE in 1 CARTON (50580-472-01) / 24 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": "21c39261-4b98-bc43-e063-6394a90a4eb8", "openfda": {"upc": ["0300450406026"], "unii": ["362O9ITL9D"], "rxcui": ["198440", "209459"], "spl_set_id": ["0c5fdda8-5049-46de-e063-6294a90a592b"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-472-01) / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-472-01", "marketing_start_date": "20240318"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-472-02) / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-472-02", "marketing_start_date": "20240318"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-472-03) / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-472-03", "marketing_start_date": "20240318"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-472-04) / 200 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-472-04", "marketing_start_date": "20240318"}], "brand_name": "Tylenol Extra Strength", "product_id": "50580-472_21c39261-4b98-bc43-e063-6394a90a4eb8", "dosage_form": "TABLET, FILM COATED", "product_ndc": "50580-472", "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": "20240318", "listing_expiration_date": "20261231"}