acetaminophen 500 mg
Generic: acetaminophen
Labeler: nuvicare llcDrug Facts
Product Profile
Brand Name
acetaminophen 500 mg
Generic Name
acetaminophen
Labeler
nuvicare llc
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
84324-003
Product ID
84324-003_d807f30b-98b7-47af-b1b9-fa01e660ffff
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2024-07-17
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84324003
Hyphenated Format
84324-003
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
acetaminophen 500 mg (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 (84324-003-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d807f30b-98b7-47af-b1b9-fa01e660ffff", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["95edf7bd-b6a7-4be5-9ad7-8748e7c2d06e"], "manufacturer_name": ["NUVICARE LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (84324-003-01)", "package_ndc": "84324-003-01", "marketing_start_date": "20240717"}], "brand_name": "ACETAMINOPHEN 500 MG", "product_id": "84324-003_d807f30b-98b7-47af-b1b9-fa01e660ffff", "dosage_form": "TABLET", "product_ndc": "84324-003", "generic_name": "ACETAMINOPHEN", "labeler_name": "NUVICARE LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN 500 MG", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240717", "listing_expiration_date": "20261231"}