uline acetaminophen extra strength

Generic: acetaminophen

Labeler: uline
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name uline acetaminophen extra strength
Generic Name acetaminophen
Labeler uline
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Uline

Identifiers & Regulatory

Product NDC 69790-804
Product ID 69790-804_3e5d8ade-be5f-4cfa-e063-6394a90a99f6
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2019-10-07

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69790804
Hyphenated Format 69790-804

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 uline acetaminophen extra strength (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
  • 50 PACKET in 1 BOX (69790-804-33) / 2 TABLET, FILM COATED in 1 PACKET
source: ndc

Packages (1)

69790-804-33 50 PACKET in 1 BOX (69790-804-33) / 2 TABLET, FILM COATED in 1 PACKET

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Uline Acetaminophen Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3e5d8ade-be5f-4cfa-e063-6394a90a99f6", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["90167594-0a49-2492-e053-2a95a90a1401"], "manufacturer_name": ["Uline"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 PACKET in 1 BOX (69790-804-33)  / 2 TABLET, FILM COATED in 1 PACKET", "package_ndc": "69790-804-33", "marketing_start_date": "20191007"}], "brand_name": "Uline Acetaminophen Extra Strength", "product_id": "69790-804_3e5d8ade-be5f-4cfa-e063-6394a90a99f6", "dosage_form": "TABLET, FILM COATED", "product_ndc": "69790-804", "generic_name": "acetaminophen", "labeler_name": "Uline", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Uline Acetaminophen Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191007", "listing_expiration_date": "20261231"}