extra strength pain relief

Generic: acetaminophen

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name extra strength pain relief
Generic Name acetaminophen
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8786
Product ID 68788-8786_5ef18daa-ac7f-42af-9cbb-fec8469f2161
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Marketing Start 2024-12-12
Marketing End 2026-11-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888786
Hyphenated Format 68788-8786

Supplemental Identifiers

RxCUI
198440
UNII
362O9ITL9D

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 extra strength pain relief (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 in 1 BOTTLE (68788-8786-1)
  • 20 TABLET in 1 BOTTLE (68788-8786-2)
  • 30 TABLET in 1 BOTTLE (68788-8786-3)
  • 50 TABLET in 1 BOTTLE (68788-8786-5)
source: ndc

Packages (4)

68788-8786-1 100 TABLET in 1 BOTTLE (68788-8786-1) 68788-8786-2 20 TABLET in 1 BOTTLE (68788-8786-2) 68788-8786-3 30 TABLET in 1 BOTTLE (68788-8786-3) 68788-8786-5 50 TABLET in 1 BOTTLE (68788-8786-5)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Extra Strength Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5ef18daa-ac7f-42af-9cbb-fec8469f2161", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["c70e3b8e-071d-4b9a-9393-ad8aa09c6b6e"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8786-1)", "package_ndc": "68788-8786-1", "marketing_end_date": "20261128", "marketing_start_date": "20241212"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-8786-2)", "package_ndc": "68788-8786-2", "marketing_end_date": "20261128", "marketing_start_date": "20241212"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8786-3)", "package_ndc": "68788-8786-3", "marketing_end_date": "20261128", "marketing_start_date": "20241212"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (68788-8786-5)", "package_ndc": "68788-8786-5", "marketing_end_date": "20261128", "marketing_start_date": "20241212"}], "brand_name": "Extra Strength Pain Relief", "product_id": "68788-8786_5ef18daa-ac7f-42af-9cbb-fec8469f2161", "dosage_form": "TABLET", "product_ndc": "68788-8786", "generic_name": "Acetaminophen", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261128", "marketing_start_date": "20241212"}