acetaminophen

Generic: acetaminophen

Labeler: target corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler target corporation
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
TARGET CORPORATION

Identifiers & Regulatory

Product NDC 11673-342
Product ID 11673-342_21331bbe-9573-2909-e063-6294a90abcee
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2019-06-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673342
Hyphenated Format 11673-342

Supplemental Identifiers

RxCUI
198440
UNII
362O9ITL9D

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (11673-342-01)
  • 225 TABLET, FILM COATED in 1 BOTTLE (11673-342-26)
  • 24 TABLET, FILM COATED in 1 BOTTLE (11673-342-42)
source: ndc

Packages (3)

11673-342-01 100 TABLET, FILM COATED in 1 BOTTLE (11673-342-01) 11673-342-26 225 TABLET, FILM COATED in 1 BOTTLE (11673-342-26) 11673-342-42 24 TABLET, FILM COATED in 1 BOTTLE (11673-342-42)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

ACETAMINOPHEN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "21331bbe-9573-2909-e063-6294a90abcee", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["80da2582-1a20-e111-e053-2991aa0acf32"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (11673-342-01)", "package_ndc": "11673-342-01", "marketing_start_date": "20190601"}, {"sample": false, "description": "225 TABLET, FILM COATED in 1 BOTTLE (11673-342-26)", "package_ndc": "11673-342-26", "marketing_start_date": "20190601"}, {"sample": false, "description": "24 TABLET, FILM COATED in 1 BOTTLE (11673-342-42)", "package_ndc": "11673-342-42", "marketing_start_date": "20190601"}], "brand_name": "ACETAMINOPHEN", "product_id": "11673-342_21331bbe-9573-2909-e063-6294a90abcee", "dosage_form": "TABLET, FILM COATED", "product_ndc": "11673-342", "generic_name": "ACETAMINOPHEN", "labeler_name": "TARGET CORPORATION", "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": "20190601", "listing_expiration_date": "20261231"}