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 71335-1536
Product ID 71335-1536_d69fbe1a-7339-4359-a396-d523362ab167
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 713351536
Hyphenated Format 71335-1536

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
  • 250 TABLET in 1 BOTTLE (71335-1536-0)
  • 20 TABLET in 1 BOTTLE (71335-1536-1)
  • 15 TABLET in 1 BOTTLE (71335-1536-2)
  • 40 TABLET in 1 BOTTLE (71335-1536-3)
  • 100 TABLET in 1 BOTTLE (71335-1536-4)
  • 30 TABLET in 1 BOTTLE (71335-1536-5)
  • 45 TABLET in 1 BOTTLE (71335-1536-6)
  • 50 TABLET in 1 BOTTLE (71335-1536-7)
  • 60 TABLET in 1 BOTTLE (71335-1536-8)
  • 90 TABLET in 1 BOTTLE (71335-1536-9)
source: ndc

Packages (10)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d69fbe1a-7339-4359-a396-d523362ab167", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["77fb237f-28b5-486b-b9ef-cb324d5cc0bd"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "250 TABLET in 1 BOTTLE (71335-1536-0)", "package_ndc": "71335-1536-0", "marketing_start_date": "20240530"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-1536-1)", "package_ndc": "71335-1536-1", "marketing_start_date": "20240530"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-1536-2)", "package_ndc": "71335-1536-2", "marketing_start_date": "20240530"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-1536-3)", "package_ndc": "71335-1536-3", "marketing_start_date": "20240530"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1536-4)", "package_ndc": "71335-1536-4", "marketing_start_date": "20200417"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1536-5)", "package_ndc": "71335-1536-5", "marketing_start_date": "20200616"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (71335-1536-6)", "package_ndc": "71335-1536-6", "marketing_start_date": "20240530"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (71335-1536-7)", "package_ndc": "71335-1536-7", "marketing_start_date": "20240530"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1536-8)", "package_ndc": "71335-1536-8", "marketing_start_date": "20240530"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1536-9)", "package_ndc": "71335-1536-9", "marketing_start_date": "20240530"}], "brand_name": "Acetaminophen", "product_id": "71335-1536_d69fbe1a-7339-4359-a396-d523362ab167", "dosage_form": "TABLET", "product_ndc": "71335-1536", "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"}