acetaminophen extra strength

Generic: acetaminophen

Labeler: time cap labs inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen extra strength
Generic Name acetaminophen
Labeler time cap labs inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
TIME CAP LABS INC

Identifiers & Regulatory

Product NDC 49483-341
Product ID 49483-341_3861fde3-66fe-f10c-e063-6394a90addc0
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2011-07-18

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49483341
Hyphenated Format 49483-341

Supplemental Identifiers

RxCUI
198440
UPC
0349483341201
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 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
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-341-01)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (49483-341-10)
  • 200 TABLET, FILM COATED in 1 BOTTLE (49483-341-20)
  • 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-341-50)
source: ndc

Packages (4)

49483-341-01 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-341-01) 49483-341-10 1000 TABLET, FILM COATED in 1 BOTTLE (49483-341-10) 49483-341-20 200 TABLET, FILM COATED in 1 BOTTLE (49483-341-20) 49483-341-50 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-341-50)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

ACETAMINOPHEN Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3861fde3-66fe-f10c-e063-6394a90addc0", "openfda": {"upc": ["0349483341201"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["fd24d0e0-4f36-42d3-9149-2fb957690305"], "manufacturer_name": ["TIME CAP LABS INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-341-01)", "package_ndc": "49483-341-01", "marketing_start_date": "20181217"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (49483-341-10)", "package_ndc": "49483-341-10", "marketing_start_date": "20220120"}, {"sample": false, "description": "200 TABLET, FILM COATED in 1 BOTTLE (49483-341-20)", "package_ndc": "49483-341-20", "marketing_start_date": "20231025"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-341-50)", "package_ndc": "49483-341-50", "marketing_start_date": "20210520"}], "brand_name": "ACETAMINOPHEN Extra Strength", "product_id": "49483-341_3861fde3-66fe-f10c-e063-6394a90addc0", "dosage_form": "TABLET, FILM COATED", "product_ndc": "49483-341", "generic_name": "ACETAMINOPHEN", "labeler_name": "TIME CAP LABS INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110718", "listing_expiration_date": "20261231"}