Package 36800-466-50

Brand: pain reliever pm extra strength

Generic: acetaminophen, diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 36800-466-50
Digits Only 3680046650
Product NDC 36800-466
Product ID 36800-466_a9dfaecc-0044-44bd-8b53-e6e02f4ed626
Description

1 BOTTLE, PLASTIC in 1 BOX (36800-466-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2021-11-05
Brand pain reliever pm extra strength
Generic acetaminophen, diphenhydramine hcl
Sample Package No

Linked Drug Pages (1)

Pain Reliever PM Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a9dfaecc-0044-44bd-8b53-e6e02f4ed626", "openfda": {"upc": ["0036800251410"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["923b443d-73cc-4c52-92e4-a075786b1ae3"], "manufacturer_name": ["TOP CARE (Topco Associates LLC)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (36800-466-10)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "36800-466-10", "marketing_start_date": "20211105"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (36800-466-50)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "36800-466-50", "marketing_start_date": "20211105"}], "brand_name": "Pain Reliever PM Extra Strength", "product_id": "36800-466_a9dfaecc-0044-44bd-8b53-e6e02f4ed626", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "36800-466", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "TOP CARE (Topco Associates 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_start_date": "20211105", "listing_expiration_date": "20261231"}