United States · FDA National Drug Code directory
Probenecid
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 10135-541_43e0b999-0f40-3c9d-e063-6294a90ae477
- Product NDC
- 10135-541
- Form
- TABLET, FILM COATED
- Composition / generic term
- Probenecid
- Labeler
- Marlex Pharmaceuticals Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19760729
- Source listing expiry
- 20261231
Source-listed ingredients
- PROBENECID — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (10135-541-01) · 10135-541-01
- 1000 TABLET, FILM COATED in 1 BOTTLE (10135-541-10) · 10135-541-10
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →