Package 59726-494-50

Brand: pain relief extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 59726-494-50
Digits Only 5972649450
Product NDC 59726-494
Description

1 BOTTLE, PLASTIC in 1 BOX (59726-494-50) / 50 TABLET in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2026-12-31
Brand pain relief 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": "911f8255-5be5-4012-b398-f2c9e74dc4a8", "openfda": {"upc": ["0359726020503"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["59eb14a5-40b0-4331-beb5-7166e6cdf411"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-494-05)  / 500 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "59726-494-05", "marketing_end_date": "20261231", "marketing_start_date": "20160331"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (59726-494-10)", "package_ndc": "59726-494-10", "marketing_end_date": "20261231", "marketing_start_date": "20160331"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-494-24)  / 24 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "59726-494-24", "marketing_end_date": "20261231", "marketing_start_date": "20160331"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-494-50)  / 50 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "59726-494-50", "marketing_end_date": "20261231", "marketing_start_date": "20160331"}], "brand_name": "Pain Relief Extra Strength", "product_id": "59726-494_911f8255-5be5-4012-b398-f2c9e74dc4a8", "dosage_form": "TABLET", "product_ndc": "59726-494", "generic_name": "Acetaminophen", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261231", "marketing_start_date": "20160331"}