14803-281

Generic: acetaminophen

Labeler: elysium pharmaceuticals ltd.
NDC Directory HUMAN OTC DRUG DRUG FOR FURTHER PROCESSING Active

Drug Facts

Product Profile

Brand Name
Generic Name acetaminophen
Labeler elysium pharmaceuticals ltd.
Dosage Form TABLET
Active Ingredients

acetaminophen 500 mg/1

Identifiers & Regulatory

Product NDC 14803-281
Product ID 14803-281_407c5103-ada8-52d9-e063-6394a90a31b4
Product Type HUMAN OTC DRUG
Marketing Category DRUG FOR FURTHER PROCESSING
Listing Expiration 2026-12-31
Marketing Start 2024-03-07

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 14803281
Hyphenated Format 14803-281

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: label)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: label)
Routes
oral
source: label

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 31000 TABLET in 1 BOTTLE (14803-281-00)
source: ndc

Packages (1)

14803-281-00 31000 TABLET in 1 BOTTLE (14803-281-00)

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 
{"spl_id": "407c5103-ada8-52d9-e063-6394a90a31b4", "openfda": {}, "finished": false, "packaging": [{"description": "31000 TABLET in 1 BOTTLE (14803-281-00)", "package_ndc": "14803-281-00", "marketing_start_date": "07-MAR-24"}], "product_id": "14803-281_407c5103-ada8-52d9-e063-6394a90a31b4", "dosage_form": "TABLET", "product_ndc": "14803-281", "generic_name": "Acetaminophen", "labeler_name": "Elysium Pharmaceuticals Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": null, "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_start_date": "20240307", "listing_expiration_date": "20261231"}