acetaminophen extra strength

Generic: acetaminophen

Labeler: kroger company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen extra strength
Generic Name acetaminophen
Labeler kroger company
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
KROGER COMPANY

Identifiers & Regulatory

Product NDC 30142-068
Product ID 30142-068_b65ad8d1-ef17-490d-96c0-0ea6096bf684
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2021-02-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 30142068
Hyphenated Format 30142-068

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 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 in 1 CARTON (30142-068-07) / 24 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (30142-068-24) / 100 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (30142-068-35) / 225 TABLET in 1 BOTTLE
source: ndc

Packages (3)

30142-068-07 1 BOTTLE in 1 CARTON (30142-068-07) / 24 TABLET in 1 BOTTLE 30142-068-24 1 BOTTLE in 1 CARTON (30142-068-24) / 100 TABLET in 1 BOTTLE 30142-068-35 1 BOTTLE in 1 CARTON (30142-068-35) / 225 TABLET in 1 BOTTLE

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Acetaminophen Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b65ad8d1-ef17-490d-96c0-0ea6096bf684", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["b96a2280-ec4f-7c61-e053-2995a90a18bb"], "manufacturer_name": ["KROGER COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-068-07)  / 24 TABLET in 1 BOTTLE", "package_ndc": "30142-068-07", "marketing_start_date": "20210204"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-068-24)  / 100 TABLET in 1 BOTTLE", "package_ndc": "30142-068-24", "marketing_start_date": "20240422"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-068-35)  / 225 TABLET in 1 BOTTLE", "package_ndc": "30142-068-35", "marketing_start_date": "20210426"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "30142-068_b65ad8d1-ef17-490d-96c0-0ea6096bf684", "dosage_form": "TABLET", "product_ndc": "30142-068", "generic_name": "Acetaminophen", "labeler_name": "KROGER COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210204", "listing_expiration_date": "20261231"}