pain reliever
Generic: acetaminophen
Labeler: hhh pharma usa llcDrug Facts
Product Profile
Brand Name
pain reliever
Generic Name
acetaminophen
Labeler
hhh pharma usa llc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
83586-107
Product ID
83586-107_3c2a38d8-ebf4-bc51-e063-6294a90a3556
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2025-08-12
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83586107
Hyphenated Format
83586-107
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, FILM COATED in 1 BOTTLE (83586-107-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c2a38d8-ebf4-bc51-e063-6294a90a3556", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["0c66b05d-132d-4c79-abfe-415fd68bbb9c"], "manufacturer_name": ["HHH PHARMA USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (83586-107-01)", "package_ndc": "83586-107-01", "marketing_start_date": "20250812"}], "brand_name": "Pain Reliever", "product_id": "83586-107_3c2a38d8-ebf4-bc51-e063-6294a90a3556", "dosage_form": "TABLET, FILM COATED", "product_ndc": "83586-107", "generic_name": "Acetaminophen", "labeler_name": "HHH PHARMA USA LLC", "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": "20250812", "listing_expiration_date": "20261231"}