acetaminophen
Generic: acetaminophen
Labeler: wildman business groupDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
wildman business group
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
84269-2522
Product ID
84269-2522_df0b3333-813c-483c-9e44-7a1b3b70d7b1
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2024-05-20
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
842692522
Hyphenated Format
84269-2522
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
- 50 PACKET in 1 BOX (84269-2522-1) / 2 TABLET in 1 PACKET
- 125 PACKET in 1 BOX (84269-2522-2) / 2 TABLET in 1 PACKET
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "df0b3333-813c-483c-9e44-7a1b3b70d7b1", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["943c8f49-e65e-40bc-b364-3274df4d21a2"], "manufacturer_name": ["Wildman Business Group"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 PACKET in 1 BOX (84269-2522-1) / 2 TABLET in 1 PACKET", "package_ndc": "84269-2522-1", "marketing_start_date": "20240520"}, {"sample": false, "description": "125 PACKET in 1 BOX (84269-2522-2) / 2 TABLET in 1 PACKET", "package_ndc": "84269-2522-2", "marketing_start_date": "20240520"}], "brand_name": "Acetaminophen", "product_id": "84269-2522_df0b3333-813c-483c-9e44-7a1b3b70d7b1", "dosage_form": "TABLET", "product_ndc": "84269-2522", "generic_name": "Acetaminophen", "labeler_name": "Wildman Business Group", "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": "20240520", "listing_expiration_date": "20261231"}