acetaminophen 500 mg

Generic: acetaminophen

Labeler: asclemed usa inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen 500 mg
Generic Name acetaminophen
Labeler asclemed usa inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
ASCLEMED USA INC.

Identifiers & Regulatory

Product NDC 76420-488
Product ID 76420-488_411a7984-fff2-6710-e063-6394a90a1704
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2015-11-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420488
Hyphenated Format 76420-488

Supplemental Identifiers

RxCUI
198440
UNII
362O9ITL9D

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 500 mg (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 in 1 BOTTLE, PLASTIC (76420-488-01)
  • 10 TABLET in 1 BOTTLE, PLASTIC (76420-488-10)
  • 20 TABLET in 1 BOTTLE, PLASTIC (76420-488-20)
  • 30 TABLET in 1 BOTTLE, PLASTIC (76420-488-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (76420-488-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (76420-488-90)
source: ndc

Packages (6)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "411a7984-fff2-6710-e063-6394a90a1704", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["db8e6702-88ac-4db2-9dd8-7d0ed997c2b5"], "manufacturer_name": ["ASCLEMED USA INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (76420-488-01)", "package_ndc": "76420-488-01", "marketing_start_date": "20251014"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (76420-488-10)", "package_ndc": "76420-488-10", "marketing_start_date": "20251014"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (76420-488-20)", "package_ndc": "76420-488-20", "marketing_start_date": "20251014"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (76420-488-30)", "package_ndc": "76420-488-30", "marketing_start_date": "20251014"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (76420-488-60)", "package_ndc": "76420-488-60", "marketing_start_date": "20251014"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (76420-488-90)", "package_ndc": "76420-488-90", "marketing_start_date": "20251014"}], "brand_name": "ACETAMINOPHEN 500 MG", "product_id": "76420-488_411a7984-fff2-6710-e063-6394a90a1704", "dosage_form": "TABLET", "product_ndc": "76420-488", "generic_name": "ACETAMINOPHEN", "labeler_name": "ASCLEMED USA INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN 500 MG", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20151101", "listing_expiration_date": "20261231"}