acetaminophen

Generic: acetaminophen

Labeler: granules pharmaceuticals inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler granules pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Granules Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 70010-161
Product ID 70010-161_31c4de05-74c3-ddc3-e063-6394a90a9388
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2022-02-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70010161
Hyphenated Format 70010-161

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
  • 1 BOTTLE in 1 CARTON (70010-161-01) / 100 TABLET in 1 BOTTLE
  • 500 TABLET in 1 BOTTLE (70010-161-05)
  • 1000 TABLET in 1 BOTTLE (70010-161-10)
source: ndc

Packages (3)

70010-161-01 1 BOTTLE in 1 CARTON (70010-161-01) / 100 TABLET in 1 BOTTLE 70010-161-05 500 TABLET in 1 BOTTLE (70010-161-05) 70010-161-10 1000 TABLET in 1 BOTTLE (70010-161-10)

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": "31c4de05-74c3-ddc3-e063-6394a90a9388", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["d5d49146-665e-4a93-e053-2995a90aca59"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70010-161-01)  / 100 TABLET in 1 BOTTLE", "package_ndc": "70010-161-01", "marketing_start_date": "20220215"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70010-161-05)", "package_ndc": "70010-161-05", "marketing_start_date": "20220215"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (70010-161-10)", "package_ndc": "70010-161-10", "marketing_start_date": "20220215"}], "brand_name": "ACETAMINOPHEN", "product_id": "70010-161_31c4de05-74c3-ddc3-e063-6394a90a9388", "dosage_form": "TABLET", "product_ndc": "70010-161", "generic_name": "ACETAMINOPHEN", "labeler_name": "Granules Pharmaceuticals 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": "20220215", "listing_expiration_date": "20261231"}