acetaminophen gelcaps

Generic: acetaminophen

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

Drug Facts

Product Profile

Brand Name acetaminophen gelcaps
Generic Name acetaminophen
Labeler target corporation
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
TARGET CORPORATION

Identifiers & Regulatory

Product NDC 11673-674
Product ID 11673-674_3fea737d-9911-6c9a-e063-6294a90a9664
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2027-12-31
Marketing Start 2025-07-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673674
Hyphenated Format 11673-674

Supplemental Identifiers

RxCUI
198440
UPC
0311673674345
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 gelcaps (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
  • 1 BOTTLE in 1 CARTON (11673-674-05) / 50 TABLET in 1 BOTTLE
  • 225 TABLET in 1 BOTTLE (11673-674-34)
  • 1 BOTTLE in 1 CARTON (11673-674-42) / 24 TABLET in 1 BOTTLE
  • 100 TABLET in 1 BOTTLE (11673-674-73)
source: ndc

Packages (4)

11673-674-05 1 BOTTLE in 1 CARTON (11673-674-05) / 50 TABLET in 1 BOTTLE 11673-674-34 225 TABLET in 1 BOTTLE (11673-674-34) 11673-674-42 1 BOTTLE in 1 CARTON (11673-674-42) / 24 TABLET in 1 BOTTLE 11673-674-73 100 TABLET in 1 BOTTLE (11673-674-73)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Acetaminophen gelcaps ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3fea737d-9911-6c9a-e063-6294a90a9664", "openfda": {"upc": ["0311673674345"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["2ea1931e-334e-a551-e063-6394a90a03b9"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-674-05)  / 50 TABLET in 1 BOTTLE", "package_ndc": "11673-674-05", "marketing_start_date": "20250710"}, {"sample": false, "description": "225 TABLET in 1 BOTTLE (11673-674-34)", "package_ndc": "11673-674-34", "marketing_start_date": "20250710"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-674-42)  / 24 TABLET in 1 BOTTLE", "package_ndc": "11673-674-42", "marketing_start_date": "20250710"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (11673-674-73)", "package_ndc": "11673-674-73", "marketing_start_date": "20250710"}], "brand_name": "Acetaminophen gelcaps", "product_id": "11673-674_3fea737d-9911-6c9a-e063-6294a90a9664", "dosage_form": "TABLET", "product_ndc": "11673-674", "generic_name": "Acetaminophen", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen gelcaps", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250710", "listing_expiration_date": "20271231"}