pain reliever
Generic: acetaminophen
Labeler: magno-humphries, inc.Drug Facts
Product Profile
Brand Name
pain reliever
Generic Name
acetaminophen
Labeler
magno-humphries, inc.
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
54257-473
Product ID
54257-473_08bf6b23-2a85-3732-e063-6294a90a2305
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2020-01-24
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
54257473
Hyphenated Format
54257-473
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
pain reliever (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (54257-473-02)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "08bf6b23-2a85-3732-e063-6294a90a2305", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["9d22bedb-9fb3-8421-e053-2a95a90acf4a"], "manufacturer_name": ["Magno-Humphries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (54257-473-02)", "package_ndc": "54257-473-02", "marketing_start_date": "20200124"}], "brand_name": "Pain Reliever", "product_id": "54257-473_08bf6b23-2a85-3732-e063-6294a90a2305", "dosage_form": "TABLET", "product_ndc": "54257-473", "generic_name": "ACETAMINOPHEN", "labeler_name": "Magno-Humphries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200124", "listing_expiration_date": "20261231"}