Package 50580-692-03

Brand: tylenol extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 50580-692-03
Digits Only 5058069203
Product NDC 50580-692
Description

1 BOTTLE in 1 CARTON (50580-692-03) / 225 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2018-08-06
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": "21c193b9-6b79-f35c-e063-6394a90adbfe", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440", "209459"], "spl_set_id": ["dd87e342-b0cb-4111-9f15-415dbcda4b77"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-692-01)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-692-01", "marketing_start_date": "20180806"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-692-02)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-692-02", "marketing_start_date": "20180806"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-692-03)  / 225 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-692-03", "marketing_start_date": "20180806"}], "brand_name": "TYLENOL Extra Strength", "product_id": "50580-692_21c193b9-6b79-f35c-e063-6394a90adbfe", "dosage_form": "TABLET, FILM COATED", "product_ndc": "50580-692", "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": "20180806", "listing_expiration_date": "20261231"}