Package 62011-0420-1

Brand: pain reliever pm extra strength

Generic: acetaminophen, diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 62011-0420-1
Digits Only 6201104201
Product NDC 62011-0420
Description

1 BOTTLE, PLASTIC in 1 BOX (62011-0420-1) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2026-11-29
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": "93fd7776-314e-462d-a576-d2f622d3b65b", "openfda": {"upc": ["0052569142882"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["997eb228-09cb-47ad-acbb-363b05c67635"], "manufacturer_name": ["Strategic Sourcing Services LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (62011-0420-1)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "62011-0420-1", "marketing_end_date": "20261129", "marketing_start_date": "20191129"}], "brand_name": "Pain Reliever PM Extra Strength", "product_id": "62011-0420_93fd7776-314e-462d-a576-d2f622d3b65b", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "62011-0420", "generic_name": "Acetaminophen, Diphenhydramine HCL", "labeler_name": "Strategic Sourcing Services 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": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261129", "marketing_start_date": "20191129"}