acetaminophen

Generic: acetaminophen

Labeler: velocity pharma llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH NOT FINAL Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler velocity pharma llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Velocity Pharma LLC

Identifiers & Regulatory

Product NDC 76168-120
Product ID 76168-120_6c311047-4be7-44ad-e053-2a91aa0ad047
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH NOT FINAL
Application Number part343
Listing Expiration 2026-12-31
Marketing Start 2018-05-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76168120
Hyphenated Format 76168-120

Supplemental Identifiers

RxCUI
198440
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 part343 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 60 CARTON in 1 BOTTLE (76168-120-10) / 1 TABLET in 1 CARTON
source: ndc

Packages (1)

76168-120-10 60 CARTON in 1 BOTTLE (76168-120-10) / 1 TABLET in 1 CARTON

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": "6c311047-4be7-44ad-e053-2a91aa0ad047", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["bba2ddc5-19e0-4f11-8ff7-7dd7c2d53b50"], "manufacturer_name": ["Velocity Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CARTON in 1 BOTTLE (76168-120-10)  / 1 TABLET in 1 CARTON", "package_ndc": "76168-120-10", "marketing_start_date": "20180514"}], "brand_name": "Acetaminophen", "product_id": "76168-120_6c311047-4be7-44ad-e053-2a91aa0ad047", "dosage_form": "TABLET", "product_ndc": "76168-120", "generic_name": "Acetaminophen", "labeler_name": "Velocity Pharma LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "part343", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "20180514", "listing_expiration_date": "20261231"}