acetaminophen gelcaps extra strength

Generic: acetaminophen

Labeler: united natural foods, inc. dba unfi
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen gelcaps extra strength
Generic Name acetaminophen
Labeler united natural foods, inc. dba unfi
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
United Natural Foods, Inc. dba UNFI

Identifiers & Regulatory

Product NDC 41163-520
Product ID 41163-520_24b1c980-fa47-ab5b-e063-6394a90ab3be
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2014-10-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 41163520
Hyphenated Format 41163-520

Supplemental Identifiers

RxCUI
198440
UPC
0041163467248
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 extra strength (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, PLASTIC in 1 CARTON (41163-520-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (41163-520-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "24b1c980-fa47-ab5b-e063-6394a90ab3be", "openfda": {"upc": ["0041163467248"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["3588a3ef-a493-43ed-96e0-c259f0d087db"], "manufacturer_name": ["United Natural Foods, Inc. dba UNFI"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (41163-520-01)  / 24 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "41163-520-01", "marketing_start_date": "20141101"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (41163-520-03)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "41163-520-03", "marketing_start_date": "20141001"}], "brand_name": "Acetaminophen Gelcaps Extra Strength", "product_id": "41163-520_24b1c980-fa47-ab5b-e063-6394a90ab3be", "dosage_form": "TABLET, COATED", "product_ndc": "41163-520", "generic_name": "Acetaminophen", "labeler_name": "United Natural Foods, Inc. dba UNFI", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen Gelcaps", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20141001", "listing_expiration_date": "20261231"}