pain reliever extra strength

Generic: acetaminophen

Labeler: marc glassman, 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 marc glassman, inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Marc Glassman, Inc.

Identifiers & Regulatory

Product NDC 68998-004
Product ID 68998-004_28735d9d-6830-a776-e063-6394a90a9b8d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Marketing Start 2008-03-01
Marketing End 2027-03-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68998004
Hyphenated Format 68998-004

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 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
  • 500 TABLET, COATED in 1 BOTTLE, PLASTIC (68998-004-06)
source: ndc

Packages (1)

68998-004-06 500 TABLET, COATED in 1 BOTTLE, PLASTIC (68998-004-06)

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": "28735d9d-6830-a776-e063-6394a90a9b8d", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["43bf297f-2832-424f-a013-4bfa1d6c03e6"], "manufacturer_name": ["Marc Glassman, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE, PLASTIC (68998-004-06)", "package_ndc": "68998-004-06", "marketing_end_date": "20270331", "marketing_start_date": "20080301"}], "brand_name": "Pain Reliever Extra Strength", "product_id": "68998-004_28735d9d-6830-a776-e063-6394a90a9b8d", "dosage_form": "TABLET, COATED", "product_ndc": "68998-004", "generic_name": "Acetaminophen", "labeler_name": "Marc Glassman, 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_end_date": "20270331", "marketing_start_date": "20080301"}