medline
Generic: acetaminophen
Labeler: medline industries, lpDrug Facts
Product Profile
Brand Name
medline
Generic Name
acetaminophen
Labeler
medline industries, lp
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
53329-196
Product ID
53329-196_3855ea8e-101a-b22b-e063-6294a90a086a
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2024-02-29
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
53329196
Hyphenated Format
53329-196
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
medline (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (53329-196-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3855ea8e-101a-b22b-e063-6294a90a086a", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["fc5f5dcf-53a6-538d-e053-6394a90a4583"], "manufacturer_name": ["Medline Industries, LP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (53329-196-30)", "package_ndc": "53329-196-30", "marketing_start_date": "20240229"}], "brand_name": "Medline", "product_id": "53329-196_3855ea8e-101a-b22b-e063-6294a90a086a", "dosage_form": "TABLET", "product_ndc": "53329-196", "generic_name": "acetaminophen", "labeler_name": "Medline Industries, LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Medline", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240229", "listing_expiration_date": "20261231"}