acetaminophen

Generic: acetaminophen

Labeler: a-s medication solutions
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5350
Product ID 50090-5350_987708d0-122e-47da-8591-0a0ea7979aad
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 500905350
Hyphenated Format 50090-5350

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
  • 42 TABLET in 1 BOTTLE (50090-5350-1)
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "987708d0-122e-47da-8591-0a0ea7979aad", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["c4f0f591-8501-4c6d-bf8e-ca3068ff65b5"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "42 TABLET in 1 BOTTLE (50090-5350-1)", "package_ndc": "50090-5350-1", "marketing_start_date": "20211208"}], "brand_name": "Acetaminophen", "product_id": "50090-5350_987708d0-122e-47da-8591-0a0ea7979aad", "dosage_form": "TABLET", "product_ndc": "50090-5350", "generic_name": "Acetaminophen", "labeler_name": "A-S Medication Solutions", "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"}