Package 50580-451-70

Brand: tylenol extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 50580-451-70
Digits Only 5058045170
Product NDC 50580-451
Description

700 TABLET, COATED in 1 BOTTLE, PLASTIC (50580-451-70)

Marketing

Marketing Status
Marketed Since 1994-08-19
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": "2d87c8e1-e743-56cc-e063-6394a90aac79", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440", "209459"], "spl_set_id": ["bb6533e5-e6a9-488c-b8ab-a6a06e87ede9"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50580-451-50)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50580-451-50", "marketing_start_date": "19940819"}, {"sample": false, "description": "700 TABLET, COATED in 1 BOTTLE, PLASTIC (50580-451-70)", "package_ndc": "50580-451-70", "marketing_start_date": "19940819"}], "brand_name": "TYLENOL Extra Strength", "product_id": "50580-451_2d87c8e1-e743-56cc-e063-6394a90aac79", "dosage_form": "TABLET, COATED", "product_ndc": "50580-451", "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": "19940819", "listing_expiration_date": "20261231"}