acetaminophen

Generic: acetaminophen

Labeler: trifecta pharmaceuticals usa llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler trifecta pharmaceuticals usa llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Trifecta Pharmaceuticals USA LLC

Identifiers & Regulatory

Product NDC 69396-144
Product ID 69396-144_09935a81-941d-1499-e063-6294a90a049c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2023-08-08

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69396144
Hyphenated Format 69396-144

Supplemental Identifiers

RxCUI
198440
UPC
0860004834403
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 (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
  • 1000 TABLET in 1 BOTTLE (69396-144-01)
source: ndc

Packages (1)

69396-144-01 1000 TABLET in 1 BOTTLE (69396-144-01)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Acetaminophen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "09935a81-941d-1499-e063-6294a90a049c", "openfda": {"upc": ["0860004834403"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["09935a74-34b0-0e7c-e063-6294a90a7c83"], "manufacturer_name": ["Trifecta Pharmaceuticals USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (69396-144-01)", "package_ndc": "69396-144-01", "marketing_start_date": "20231107"}], "brand_name": "Acetaminophen", "product_id": "69396-144_09935a81-941d-1499-e063-6294a90a049c", "dosage_form": "TABLET", "product_ndc": "69396-144", "generic_name": "Acetaminophen", "labeler_name": "Trifecta Pharmaceuticals USA LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230808", "listing_expiration_date": "20261231"}