Package 81522-104-04

Brand: acetaminophen extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 81522-104-04
Digits Only 8152210404
Product NDC 81522-104
Description

1 BOTTLE, PLASTIC in 1 CARTON (81522-104-04) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2023-01-11
Brand acetaminophen 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": "24996677-f6f7-01be-e063-6394a90a10d7", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["ec6add55-f4a3-7818-e053-2a95a90aee04"], "manufacturer_name": ["FSA Store Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (81522-104-04)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "81522-104-04", "marketing_start_date": "20230111"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE, PLASTIC (81522-104-06)", "package_ndc": "81522-104-06", "marketing_start_date": "20230503"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "81522-104_24996677-f6f7-01be-e063-6394a90a10d7", "dosage_form": "TABLET, COATED", "product_ndc": "81522-104", "generic_name": "Acetaminophen", "labeler_name": "FSA Store Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230111", "listing_expiration_date": "20261231"}