pain reliever extra strength

Generic: acetaminophen

Labeler: l.n.k. international, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain reliever extra strength
Generic Name acetaminophen
Labeler l.n.k. international, inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
L.N.K. International, Inc.

Identifiers & Regulatory

Product NDC 50844-519
Product ID 50844-519_9f5e3344-4f7b-4096-a4f0-929e140c175c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2004-05-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50844519
Hyphenated Format 50844-519

Supplemental Identifiers

RxCUI
198440
UPC
0050844519213
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 pain reliever 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, COATED in 1 BOTTLE, PLASTIC (50844-519-12)
  • 225 TABLET, COATED in 1 BOTTLE, PLASTIC (50844-519-20)
  • 1 BOTTLE, PLASTIC in 1 CARTON (50844-519-21) / 16 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (3)

50844-519-12 100 TABLET, COATED in 1 BOTTLE, PLASTIC (50844-519-12) 50844-519-20 225 TABLET, COATED in 1 BOTTLE, PLASTIC (50844-519-20) 50844-519-21 1 BOTTLE, PLASTIC in 1 CARTON (50844-519-21) / 16 TABLET, COATED in 1 BOTTLE, PLASTIC

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Pain Reliever Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9f5e3344-4f7b-4096-a4f0-929e140c175c", "openfda": {"upc": ["0050844519213"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["72babe91-2586-4f05-ae90-6debfd23aa5d"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE, PLASTIC (50844-519-12)", "package_ndc": "50844-519-12", "marketing_start_date": "20231114"}, {"sample": false, "description": "225 TABLET, COATED in 1 BOTTLE, PLASTIC (50844-519-20)", "package_ndc": "50844-519-20", "marketing_start_date": "20231114"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-519-21)  / 16 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50844-519-21", "marketing_start_date": "20040510"}], "brand_name": "Pain Reliever Extra Strength", "product_id": "50844-519_9f5e3344-4f7b-4096-a4f0-929e140c175c", "dosage_form": "TABLET, COATED", "product_ndc": "50844-519", "generic_name": "Acetaminophen", "labeler_name": "L.N.K. International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20040510", "listing_expiration_date": "20261231"}