probenecid

Generic: probenecid

Labeler: marlex pharmaceuticals inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name probenecid
Generic Name probenecid
Labeler marlex pharmaceuticals inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

probenecid 500 mg/1

Manufacturer
Marlex Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 10135-541
Product ID 10135-541_43e0b999-0f40-3c9d-e063-6294a90ae477
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 10135541
Hyphenated Format 10135-541

Supplemental Identifiers

RxCUI
198152
UNII
PO572Z7917

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 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 (10135-541-01)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (10135-541-10)
source: ndc

Packages (2)

10135-541-01 100 TABLET, FILM COATED in 1 BOTTLE (10135-541-01) 10135-541-10 1000 TABLET, FILM COATED in 1 BOTTLE (10135-541-10)

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": "43e0b999-0f40-3c9d-e063-6294a90ae477", "openfda": {"unii": ["PO572Z7917"], "rxcui": ["198152"], "spl_set_id": ["5d552de5-2d18-4464-bcaf-0311fa3f080d"], "manufacturer_name": ["Marlex Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (10135-541-01)", "package_ndc": "10135-541-01", "marketing_start_date": "19760729"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (10135-541-10)", "package_ndc": "10135-541-10", "marketing_start_date": "19760729"}], "brand_name": "Probenecid", "product_id": "10135-541_43e0b999-0f40-3c9d-e063-6294a90ae477", "dosage_form": "TABLET, FILM COATED", "product_ndc": "10135-541", "generic_name": "Probenecid", "labeler_name": "Marlex Pharmaceuticals Inc", "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"}