acetaminophen

Generic: acetaminophen

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-241
Product ID 72789-241_40ad32ad-c8d2-ba2c-e063-6294a90ac94d
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 72789241
Hyphenated Format 72789-241

Supplemental Identifiers

RxCUI
198440
UPC
0372789241302
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
  • 100 TABLET in 1 BOTTLE, PLASTIC (72789-241-01)
  • 20 TABLET in 1 BOTTLE, PLASTIC (72789-241-20)
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-241-30)
  • 50 TABLET in 1 BOTTLE, PLASTIC (72789-241-50)
  • 60 TABLET in 1 BOTTLE, PLASTIC (72789-241-60)
source: ndc

Packages (5)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40ad32ad-c8d2-ba2c-e063-6294a90ac94d", "openfda": {"upc": ["0372789241302"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["3f96aeb1-a533-4d36-9a1f-62fc094b6754"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-241-01)", "package_ndc": "72789-241-01", "marketing_start_date": "20220412"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (72789-241-20)", "package_ndc": "72789-241-20", "marketing_start_date": "20220407"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-241-30)", "package_ndc": "72789-241-30", "marketing_start_date": "20220407"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE, PLASTIC (72789-241-50)", "package_ndc": "72789-241-50", "marketing_start_date": "20220412"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-241-60)", "package_ndc": "72789-241-60", "marketing_start_date": "20220407"}], "brand_name": "Acetaminophen", "product_id": "72789-241_40ad32ad-c8d2-ba2c-e063-6294a90ac94d", "dosage_form": "TABLET", "product_ndc": "72789-241", "generic_name": "Acetaminophen", "labeler_name": "PD-Rx 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": "20180912", "listing_expiration_date": "20261231"}