Package 0363-0484-76

Brand: pain reliever extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 0363-0484-76
Digits Only 0363048476
Product NDC 0363-0484
Description

1 BOTTLE in 1 CARTON (0363-0484-76) / 120 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-01-22
Brand pain reliever 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": "3e28b7c8-93bf-4e3a-9108-08c8d7d4e8d5", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["28e275fb-d615-4725-998c-946fe1bfdc0c"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0484-62)  / 24 TABLET in 1 BOTTLE", "package_ndc": "0363-0484-62", "marketing_start_date": "20220330"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0484-71)  / 50 TABLET in 1 BOTTLE", "package_ndc": "0363-0484-71", "marketing_start_date": "20220330"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0484-76)  / 120 TABLET in 1 BOTTLE", "package_ndc": "0363-0484-76", "marketing_start_date": "20250122"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0484-78)  / 100 TABLET in 1 BOTTLE", "package_ndc": "0363-0484-78", "marketing_start_date": "20220330"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0484-83)  / 225 TABLET in 1 BOTTLE", "package_ndc": "0363-0484-83", "marketing_start_date": "20220926"}], "brand_name": "Pain Reliever Extra Strength", "product_id": "0363-0484_3e28b7c8-93bf-4e3a-9108-08c8d7d4e8d5", "dosage_form": "TABLET", "product_ndc": "0363-0484", "generic_name": "Acetaminophen", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20090121", "listing_expiration_date": "20261231"}