Package 54257-278-02

Brand: pain reliever pm

Generic: acetaminophen, diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 54257-278-02
Digits Only 5425727802
Product NDC 54257-278
Description

100 TABLET in 1 BOTTLE (54257-278-02)

Marketing

Marketing Status
Marketed Since 2020-01-24
Brand pain reliever pm
Generic acetaminophen, diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "08bf29ff-1c79-1547-e063-6294a90ac7ee", "openfda": {"upc": ["0043292562405"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["9d2275c8-0c3d-d2b3-e053-2995a90a368e"], "manufacturer_name": ["Magno-Humphries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (54257-278-02)", "package_ndc": "54257-278-02", "marketing_start_date": "20200124"}], "brand_name": "Pain Reliever PM", "product_id": "54257-278_08bf29ff-1c79-1547-e063-6294a90ac7ee", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "54257-278", "generic_name": "ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "Magno-Humphries, 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": "20200124", "listing_expiration_date": "20261231"}