acetaminophen
Generic: acetaminophen
Labeler: unfiDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
unfi
Dosage Form
TABLET, COATED
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
41163-592
Product ID
41163-592_28d7b554-9423-5127-e063-6294a90a1dd2
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2022-09-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
41163592
Hyphenated Format
41163-592
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 (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (41163-592-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "28d7b554-9423-5127-e063-6294a90a1dd2", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["e689c9e3-dd4d-c646-e053-2a95a90a4b6a"], "manufacturer_name": ["UNFI"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (41163-592-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "41163-592-01", "marketing_start_date": "20220915"}], "brand_name": "acetaminophen", "product_id": "41163-592_28d7b554-9423-5127-e063-6294a90a1dd2", "dosage_form": "TABLET, COATED", "product_ndc": "41163-592", "generic_name": "Acetaminophen", "labeler_name": "UNFI", "product_type": "HUMAN OTC DRUG", "brand_name_base": "acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220915", "listing_expiration_date": "20261231"}