Package 50844-556-10

Brand: pain reliever pm extra strength

Generic: acetaminophen, diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 50844-556-10
Digits Only 5084455610
Product NDC 50844-556
Product ID 50844-556_82f8ff4b-21ec-402e-b4ae-0a25d84e2803
Description

1 BOTTLE, PLASTIC in 1 CARTON (50844-556-10) / 40 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2007-12-17
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": "82f8ff4b-21ec-402e-b4ae-0a25d84e2803", "openfda": {"upc": ["0050844556102"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["ff199db8-c7ea-4b6e-ad8b-3ceeca883d92"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-556-10)  / 40 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50844-556-10", "marketing_start_date": "20071217"}], "brand_name": "Pain Reliever PM Extra Strength", "product_id": "50844-556_82f8ff4b-21ec-402e-b4ae-0a25d84e2803", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50844-556", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "L.N.K. International, Inc.", "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": "20071217", "listing_expiration_date": "20261231"}