extra strength acetaminophen
Generic: acetaminophen
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
extra strength acetaminophen
Generic Name
acetaminophen
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-2179
Product ID
72162-2179_0148ca05-29b7-4155-8403-28dfbe09fc20
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2018-07-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721622179
Hyphenated Format
72162-2179
Supplemental Identifiers
RxCUI
UNII
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
extra strength acetaminophen (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (72162-2179-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0148ca05-29b7-4155-8403-28dfbe09fc20", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["ea417ddb-54b3-49e2-bec1-8fe450d9990c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2179-1)", "package_ndc": "72162-2179-1", "marketing_start_date": "20240202"}], "brand_name": "Extra Strength Acetaminophen", "product_id": "72162-2179_0148ca05-29b7-4155-8403-28dfbe09fc20", "dosage_form": "TABLET", "product_ndc": "72162-2179", "generic_name": "Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180701", "listing_expiration_date": "20261231"}