acetaminophen
Generic: acetaminophen
Labeler: prostat first aidDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
prostat first aid
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
58228-1986
Product ID
58228-1986_3bdbeabb-6b05-5468-e063-6394a90a03c9
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2025-08-06
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
582281986
Hyphenated Format
58228-1986
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
- 10000 PACKET in 1 BAG (58228-1986-1) / 2 TABLET in 1 PACKET
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3bdbeabb-6b05-5468-e063-6394a90a03c9", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["3bdbea6a-3f11-9142-e063-6294a90a20ea"], "manufacturer_name": ["Prostat First Aid"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10000 PACKET in 1 BAG (58228-1986-1) / 2 TABLET in 1 PACKET", "package_ndc": "58228-1986-1", "marketing_start_date": "20250806"}], "brand_name": "Acetaminophen", "product_id": "58228-1986_3bdbeabb-6b05-5468-e063-6394a90a03c9", "dosage_form": "TABLET", "product_ndc": "58228-1986", "generic_name": "Acetaminophen", "labeler_name": "Prostat First Aid", "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": "20250806", "listing_expiration_date": "20261231"}