acetaminophen
Generic: acetaminophen
Labeler: cardinal health 107, llcDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
cardinal health 107, llc
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55154-7897
Product ID
55154-7897_b59bb526-dff2-4b95-929e-931ac406ebd3
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2018-09-12
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
551547897
Hyphenated Format
55154-7897
Supplemental Identifiers
RxCUI
UPC
UNII
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
- 10 BLISTER PACK in 1 BAG (55154-7897-0) / 1 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b59bb526-dff2-4b95-929e-931ac406ebd3", "openfda": {"upc": ["0055154789707"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["9efcce86-dd57-4ea2-ad31-d2038eb61bf1"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-7897-0) / 1 TABLET in 1 BLISTER PACK", "package_ndc": "55154-7897-0", "marketing_start_date": "20180912"}], "brand_name": "Acetaminophen", "product_id": "55154-7897_b59bb526-dff2-4b95-929e-931ac406ebd3", "dosage_form": "TABLET", "product_ndc": "55154-7897", "generic_name": "Acetaminophen", "labeler_name": "Cardinal Health 107, LLC", "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": "20180912", "listing_expiration_date": "20261231"}