Package 50844-256-08

Brand: pain reliever pm

Generic: acetaminophen, diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 50844-256-08
Digits Only 5084425608
Product NDC 50844-256
Product ID 50844-256_0b04ddec-7b7f-413c-a74e-68ca4635a6b8
Description

1 BOTTLE, PLASTIC in 1 CARTON (50844-256-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2019-07-30
Brand pain reliever pm
Generic acetaminophen, diphenhydramine hcl
Sample Package No

Linked Drug Pages (1)

Pain Reliever PM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0b04ddec-7b7f-413c-a74e-68ca4635a6b8", "openfda": {"upc": ["0052548689926"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["ec902e52-0f48-4a61-b67d-17e1c1461619"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-256-08)  / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50844-256-08", "marketing_start_date": "20190730"}], "brand_name": "Pain Reliever PM", "product_id": "50844-256_0b04ddec-7b7f-413c-a74e-68ca4635a6b8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50844-256", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "L.N.K. International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever PM", "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": "20190730", "listing_expiration_date": "20261231"}