acetaminophen 500 mg

Generic: acetaminophen

Labeler: pioneer life sciences, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen 500 mg
Generic Name acetaminophen
Labeler pioneer life sciences, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Pioneer Life Sciences, LLC

Identifiers & Regulatory

Product NDC 72090-008
Product ID 72090-008_c7221f1d-d823-4514-a3a8-8d02afbb43fd
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2023-05-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72090008
Hyphenated Format 72090-008

Supplemental Identifiers

RxCUI
198440
UPC
0372090000490
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 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
  • 300 TABLET in 1 BOTTLE (72090-008-30)
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (2)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c7221f1d-d823-4514-a3a8-8d02afbb43fd", "openfda": {"upc": ["0372090000490"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["11e6ec2a-5171-4496-a15f-6ff744bd1f2f"], "manufacturer_name": ["Pioneer Life Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET in 1 BOTTLE (72090-008-30)", "package_ndc": "72090-008-30", "marketing_start_date": "20230511"}], "brand_name": "ACETAMINOPHEN 500 MG", "product_id": "72090-008_c7221f1d-d823-4514-a3a8-8d02afbb43fd", "dosage_form": "TABLET", "product_ndc": "72090-008", "generic_name": "ACETAMINOPHEN", "labeler_name": "Pioneer Life Sciences, LLC", "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": "20230511", "listing_expiration_date": "20261231"}