pain reliever
Generic: acetaminophen
Labeler: shield pharmaceuticals corpDrug Facts
Product Profile
Brand Name
pain reliever
Generic Name
acetaminophen
Labeler
shield pharmaceuticals corp
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
83059-0103
Product ID
83059-0103_43073225-59e2-7d5d-e063-6394a90a17d8
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2025-11-07
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
830590103
Hyphenated Format
83059-0103
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
- 50 TABLET in 1 BOTTLE (83059-0103-5)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "43073225-59e2-7d5d-e063-6394a90a17d8", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["61e50135-a7c2-4a86-8a1a-d47b41d3f9d1"], "manufacturer_name": ["Shield Pharmaceuticals Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (83059-0103-5)", "package_ndc": "83059-0103-5", "marketing_start_date": "20251107"}], "brand_name": "Pain Reliever", "product_id": "83059-0103_43073225-59e2-7d5d-e063-6394a90a17d8", "dosage_form": "TABLET", "product_ndc": "83059-0103", "generic_name": "Acetaminophen", "labeler_name": "Shield Pharmaceuticals Corp", "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": "20251107", "listing_expiration_date": "20261231"}