Package 59726-868-24

Brand: pain reliever pm extra strength

Generic: acetaminophen diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 59726-868-24
Digits Only 5972686824
Product NDC 59726-868
Description

1 BOTTLE, PLASTIC in 1 BOX (59726-868-24) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2026-12-26
Brand pain reliever pm extra strength
Generic acetaminophen diphenhydramine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fd04bd61-2bce-4ec0-99b0-ebd0995d3aba", "openfda": {"upc": ["0359726863100"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["90eba2e8-52c3-43f5-ba93-4a520368c7f4"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-868-10)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "59726-868-10", "marketing_end_date": "20261226", "marketing_start_date": "20210326"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-868-24)  / 24 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "59726-868-24", "marketing_end_date": "20261226", "marketing_start_date": "20210326"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-868-50)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "59726-868-50", "marketing_end_date": "20261226", "marketing_start_date": "20210326"}], "brand_name": "Pain Reliever PM extra strength", "product_id": "59726-868_fd04bd61-2bce-4ec0-99b0-ebd0995d3aba", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "59726-868", "generic_name": "Acetaminophen Diphenhydramine HCL", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever PM", "brand_name_suffix": "extra strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261226", "marketing_start_date": "20210326"}