pain relief acetaminophen extra strength

Generic: acetaminophen

Labeler: rite aid corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief acetaminophen extra strength
Generic Name acetaminophen
Labeler rite aid corporation
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Rite Aid Corporation

Identifiers & Regulatory

Product NDC 11822-0519
Product ID 11822-0519_41be6a05-0efe-4991-9ad7-b060657c4b63
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 118220519
Hyphenated Format 11822-0519

Supplemental Identifiers

RxCUI
198440
UPC
0011822041249
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 relief 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
  • 1 BOTTLE, PLASTIC in 1 CARTON (11822-0519-2) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 225 TABLET, COATED in 1 BOTTLE, PLASTIC (11822-0519-3)
  • 1 BOTTLE, PLASTIC in 1 CARTON (11822-0519-5) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (11822-0519-8) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 150 TABLET, COATED in 1 BOTTLE, PLASTIC (11822-0519-9)
source: ndc

Packages (5)

11822-0519-2 1 BOTTLE, PLASTIC in 1 CARTON (11822-0519-2) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC 11822-0519-3 225 TABLET, COATED in 1 BOTTLE, PLASTIC (11822-0519-3) 11822-0519-5 1 BOTTLE, PLASTIC in 1 CARTON (11822-0519-5) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC 11822-0519-8 1 BOTTLE, PLASTIC in 1 CARTON (11822-0519-8) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC 11822-0519-9 150 TABLET, COATED in 1 BOTTLE, PLASTIC (11822-0519-9)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

pain relief acetaminophen Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "41be6a05-0efe-4991-9ad7-b060657c4b63", "openfda": {"upc": ["0011822041249"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["26c0641e-1cdd-4084-939d-01dbd36ab9b7"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (11822-0519-2)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "11822-0519-2", "marketing_start_date": "20040510"}, {"sample": false, "description": "225 TABLET, COATED in 1 BOTTLE, PLASTIC (11822-0519-3)", "package_ndc": "11822-0519-3", "marketing_start_date": "20040510"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (11822-0519-5)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "11822-0519-5", "marketing_start_date": "20040510"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (11822-0519-8)  / 24 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "11822-0519-8", "marketing_start_date": "20040510"}, {"sample": false, "description": "150 TABLET, COATED in 1 BOTTLE, PLASTIC (11822-0519-9)", "package_ndc": "11822-0519-9", "marketing_start_date": "20040510"}], "brand_name": "pain relief acetaminophen Extra Strength", "product_id": "11822-0519_41be6a05-0efe-4991-9ad7-b060657c4b63", "dosage_form": "TABLET, COATED", "product_ndc": "11822-0519", "generic_name": "Acetaminophen", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "pain relief 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": "20040510", "listing_expiration_date": "20261231"}