extra strength pain relief

Generic: acetaminophen

Labeler: bryant ranch prepack
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name extra strength pain relief
Generic Name acetaminophen
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-1516
Product ID 63629-1516_86dfb73f-2bff-4d40-accd-422643f7358b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 1989-01-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 636291516
Hyphenated Format 63629-1516

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
  • 250 TABLET in 1 BOTTLE (63629-1516-0)
  • 20 TABLET in 1 BOTTLE (63629-1516-1)
  • 15 TABLET in 1 BOTTLE (63629-1516-2)
  • 40 TABLET in 1 BOTTLE (63629-1516-3)
  • 100 TABLET in 1 BOTTLE (63629-1516-4)
  • 30 TABLET in 1 BOTTLE (63629-1516-5)
  • 45 TABLET in 1 BOTTLE (63629-1516-6)
  • 50 TABLET in 1 BOTTLE (63629-1516-7)
  • 60 TABLET in 1 BOTTLE (63629-1516-8)
  • 90 TABLET in 1 BOTTLE (63629-1516-9)
source: ndc

Packages (10)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "86dfb73f-2bff-4d40-accd-422643f7358b", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["31a97a6a-e5c8-429a-b497-330f0d84777d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "250 TABLET in 1 BOTTLE (63629-1516-0)", "package_ndc": "63629-1516-0", "marketing_start_date": "20090904"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (63629-1516-1)", "package_ndc": "63629-1516-1", "marketing_start_date": "20080617"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (63629-1516-2)", "package_ndc": "63629-1516-2", "marketing_start_date": "20230301"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (63629-1516-3)", "package_ndc": "63629-1516-3", "marketing_start_date": "20041229"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-1516-4)", "package_ndc": "63629-1516-4", "marketing_start_date": "20060221"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-1516-5)", "package_ndc": "63629-1516-5", "marketing_start_date": "20070327"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (63629-1516-6)", "package_ndc": "63629-1516-6", "marketing_start_date": "20090811"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (63629-1516-7)", "package_ndc": "63629-1516-7", "marketing_start_date": "20080910"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63629-1516-8)", "package_ndc": "63629-1516-8", "marketing_start_date": "20081009"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63629-1516-9)", "package_ndc": "63629-1516-9", "marketing_start_date": "20101221"}], "brand_name": "Extra Strength Pain Relief", "product_id": "63629-1516_86dfb73f-2bff-4d40-accd-422643f7358b", "dosage_form": "TABLET", "product_ndc": "63629-1516", "generic_name": "Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "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_start_date": "19890101", "listing_expiration_date": "20261231"}