Package 59726-013-10

Brand: arthritis pain reliever extended release

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 59726-013-10
Digits Only 5972601310
Product NDC 59726-013
Product ID 59726-013_215e2e69-2d92-4cb7-9f64-a06bcfa7f6e3
Description

1 BOTTLE, PLASTIC in 1 BOX (59726-013-10) / 100 TABLET in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2026-04-30
Brand arthritis pain reliever extended release
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Arthritis Pain Reliever Extended Release ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "215e2e69-2d92-4cb7-9f64-a06bcfa7f6e3", "openfda": {"upc": ["0359726013109"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["0dcf54e7-de0c-426a-9b49-2ac2e8b6bdb0"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-013-10)  / 100 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "59726-013-10", "marketing_end_date": "20260430", "marketing_start_date": "20200430"}], "brand_name": "Arthritis Pain Reliever Extended Release", "product_id": "59726-013_215e2e69-2d92-4cb7-9f64-a06bcfa7f6e3", "dosage_form": "TABLET", "product_ndc": "59726-013", "generic_name": "Acetaminophen", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Arthritis Pain Reliever", "brand_name_suffix": "Extended Release", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20200430"}