acetaminophen

Generic: acetaminophen

Labeler: bryant ranch prepack
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2164
Product ID 72162-2164_ce0027c4-cd60-4e48-96ce-9a12a2113f40
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2018-09-12

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622164
Hyphenated Format 72162-2164

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 (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
  • 1 BOTTLE in 1 CARTON (72162-2164-1) / 100 TABLET in 1 BOTTLE
source: ndc

Packages (1)

72162-2164-1 1 BOTTLE in 1 CARTON (72162-2164-1) / 100 TABLET in 1 BOTTLE

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": "ce0027c4-cd60-4e48-96ce-9a12a2113f40", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["b5053cf5-209d-4106-afc2-cf9af85f4a69"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (72162-2164-1)  / 100 TABLET in 1 BOTTLE", "package_ndc": "72162-2164-1", "marketing_start_date": "20180912"}], "brand_name": "Acetaminophen", "product_id": "72162-2164_ce0027c4-cd60-4e48-96ce-9a12a2113f40", "dosage_form": "TABLET", "product_ndc": "72162-2164", "generic_name": "Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "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": "20180912", "listing_expiration_date": "20261231"}