probenecid

Generic: probenecid

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name probenecid
Generic Name probenecid
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

probenecid 500 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2237
Product ID 72162-2237_8c261b93-98b4-46ce-a713-11d3b2d7cd13
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA080966
Listing Expiration 2026-12-31
Marketing Start 1976-07-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622237
Hyphenated Format 72162-2237

Supplemental Identifiers

RxCUI
198152
UNII
PO572Z7917

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 probenecid (source: ndc)
Generic Name probenecid (source: ndc)
Application Number ANDA080966 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (72162-2237-1)
source: ndc

Packages (1)

72162-2237-1 100 TABLET, FILM COATED in 1 BOTTLE (72162-2237-1)

Ingredients (1)

probenecid (500 mg/1)

Linked Drug Pages (1)

Probenecid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8c261b93-98b4-46ce-a713-11d3b2d7cd13", "openfda": {"unii": ["PO572Z7917"], "rxcui": ["198152"], "spl_set_id": ["6aec72b5-a9f4-45a3-82a6-7d3de64ba5e5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-2237-1)", "package_ndc": "72162-2237-1", "marketing_start_date": "20240126"}], "brand_name": "Probenecid", "product_id": "72162-2237_8c261b93-98b4-46ce-a713-11d3b2d7cd13", "dosage_form": "TABLET, FILM COATED", "product_ndc": "72162-2237", "generic_name": "Probenecid", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Probenecid", "active_ingredients": [{"name": "PROBENECID", "strength": "500 mg/1"}], "application_number": "ANDA080966", "marketing_category": "ANDA", "marketing_start_date": "19760729", "listing_expiration_date": "20261231"}