acetaminophen extra strength

Generic: acetaminophen

Labeler: aurohealth llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen extra strength
Generic Name acetaminophen
Labeler aurohealth llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Aurohealth LLC

Identifiers & Regulatory

Product NDC 58602-745
Product ID 58602-745_0b44d6cf-d21e-741a-e063-6294a90a05ff
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2021-01-07

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58602745
Hyphenated Format 58602-745

Supplemental Identifiers

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 (58602-745-07) / 24 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (58602-745-14) / 50 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (58602-745-21) / 100 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (58602-745-35) / 225 TABLET in 1 BOTTLE
source: ndc

Packages (4)

58602-745-07 1 BOTTLE in 1 CARTON (58602-745-07) / 24 TABLET in 1 BOTTLE 58602-745-14 1 BOTTLE in 1 CARTON (58602-745-14) / 50 TABLET in 1 BOTTLE 58602-745-21 1 BOTTLE in 1 CARTON (58602-745-21) / 100 TABLET in 1 BOTTLE 58602-745-35 1 BOTTLE in 1 CARTON (58602-745-35) / 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": "0b44d6cf-d21e-741a-e063-6294a90a05ff", "openfda": {"unii": ["362O9ITL9D"], "spl_set_id": ["bc03fa56-8880-4bbd-81a0-91853fecdd4e"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-745-07)  / 24 TABLET in 1 BOTTLE", "package_ndc": "58602-745-07", "marketing_start_date": "20210107"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-745-14)  / 50 TABLET in 1 BOTTLE", "package_ndc": "58602-745-14", "marketing_start_date": "20210107"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-745-21)  / 100 TABLET in 1 BOTTLE", "package_ndc": "58602-745-21", "marketing_start_date": "20210107"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-745-35)  / 225 TABLET in 1 BOTTLE", "package_ndc": "58602-745-35", "marketing_start_date": "20210107"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "58602-745_0b44d6cf-d21e-741a-e063-6294a90a05ff", "dosage_form": "TABLET", "product_ndc": "58602-745", "generic_name": "Acetaminophen", "labeler_name": "Aurohealth LLC", "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": "20210107", "listing_expiration_date": "20261231"}