welby acetaminophen
Generic: acetaminophen
Labeler: aldi, incDrug Facts
Product Profile
Brand Name
welby acetaminophen
Generic Name
acetaminophen
Labeler
aldi, inc
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
64024-001
Product ID
64024-001_6ff348fd-75a4-4aea-a3a7-542e7d7a3d9c
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2016-01-05
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
64024001
Hyphenated Format
64024-001
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
welby acetaminophen (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (64024-001-78) / 100 TABLET in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6ff348fd-75a4-4aea-a3a7-542e7d7a3d9c", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["7e09702c-52d4-490d-a320-13a1ab422100"], "manufacturer_name": ["Aldi, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (64024-001-78) / 100 TABLET in 1 BOTTLE", "package_ndc": "64024-001-78", "marketing_start_date": "20160105"}], "brand_name": "welby acetaminophen", "product_id": "64024-001_6ff348fd-75a4-4aea-a3a7-542e7d7a3d9c", "dosage_form": "TABLET", "product_ndc": "64024-001", "generic_name": "Acetaminophen", "labeler_name": "Aldi, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "welby acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160105", "listing_expiration_date": "20261231"}