acetaminophen

Generic: acetaminophen

Labeler: granules usa, inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler granules usa, inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Granules USA, Inc

Identifiers & Regulatory

Product NDC 69848-003
Product ID 69848-003_468e5f4e-8bc6-6b97-e063-6294a90a0166
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2019-07-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69848003
Hyphenated Format 69848-003

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 M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69848-003-10)
  • 175 TABLET in 1 BOTTLE (69848-003-17)
  • 24 TABLET in 1 BOTTLE (69848-003-24)
source: ndc

Packages (3)

69848-003-10 100 TABLET in 1 BOTTLE (69848-003-10) 69848-003-17 175 TABLET in 1 BOTTLE (69848-003-17) 69848-003-24 24 TABLET in 1 BOTTLE (69848-003-24)

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": "468e5f4e-8bc6-6b97-e063-6294a90a0166", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["a1255f60-b9c6-9a95-e053-2995a90a9e80"], "manufacturer_name": ["Granules USA, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69848-003-10)", "package_ndc": "69848-003-10", "marketing_start_date": "20190701"}, {"sample": false, "description": "175 TABLET in 1 BOTTLE (69848-003-17)", "package_ndc": "69848-003-17", "marketing_start_date": "20190701"}, {"sample": false, "description": "24 TABLET in 1 BOTTLE (69848-003-24)", "package_ndc": "69848-003-24", "marketing_start_date": "20190701"}], "brand_name": "Acetaminophen", "product_id": "69848-003_468e5f4e-8bc6-6b97-e063-6294a90a0166", "dosage_form": "TABLET", "product_ndc": "69848-003", "generic_name": "Acetaminophen", "labeler_name": "Granules USA, Inc", "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": "20190701", "listing_expiration_date": "20261231"}