acetaminophen

Generic: acetaminophen

Labeler: proficient rx lp
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-165
Product ID 71205-165_d52d213f-141d-4f01-87c7-0692e69dbc56
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 71205165
Hyphenated Format 71205-165

Supplemental Identifiers

RxCUI
198440
UPC
0371205165505
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
  • 10 TABLET in 1 BOTTLE (71205-165-10)
  • 24 TABLET in 1 BOTTLE (71205-165-24)
  • 30 TABLET in 1 BOTTLE (71205-165-30)
  • 40 TABLET in 1 BOTTLE (71205-165-40)
  • 50 TABLET in 1 BOTTLE (71205-165-50)
  • 60 TABLET in 1 BOTTLE (71205-165-60)
  • 90 TABLET in 1 BOTTLE (71205-165-90)
source: ndc

Packages (7)

71205-165-10 10 TABLET in 1 BOTTLE (71205-165-10) 71205-165-24 24 TABLET in 1 BOTTLE (71205-165-24) 71205-165-30 30 TABLET in 1 BOTTLE (71205-165-30) 71205-165-40 40 TABLET in 1 BOTTLE (71205-165-40) 71205-165-50 50 TABLET in 1 BOTTLE (71205-165-50) 71205-165-60 60 TABLET in 1 BOTTLE (71205-165-60) 71205-165-90 90 TABLET in 1 BOTTLE (71205-165-90)

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": "d52d213f-141d-4f01-87c7-0692e69dbc56", "openfda": {"upc": ["0371205165505"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["9af5ccc8-aac0-4339-a9f6-58fdc9b91c57"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (71205-165-10)", "package_ndc": "71205-165-10", "marketing_start_date": "20181201"}, {"sample": false, "description": "24 TABLET in 1 BOTTLE (71205-165-24)", "package_ndc": "71205-165-24", "marketing_start_date": "20250424"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-165-30)", "package_ndc": "71205-165-30", "marketing_start_date": "20181201"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71205-165-40)", "package_ndc": "71205-165-40", "marketing_start_date": "20181201"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (71205-165-50)", "package_ndc": "71205-165-50", "marketing_start_date": "20181201"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-165-60)", "package_ndc": "71205-165-60", "marketing_start_date": "20181201"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-165-90)", "package_ndc": "71205-165-90", "marketing_start_date": "20181201"}], "brand_name": "Acetaminophen", "product_id": "71205-165_d52d213f-141d-4f01-87c7-0692e69dbc56", "dosage_form": "TABLET", "product_ndc": "71205-165", "generic_name": "Acetaminophen", "labeler_name": "Proficient Rx LP", "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"}