Active ingredient
Probenecid
7 finished FDA listings contain Probenecid as their only active ingredient; 5 combination products also contain it.
FDA NDC Directory
- Ingredient names as written by FDA
- PROBENECID
- Dosage forms
- Tablet, Tablet, Film Coated
- Routes
- Oral
- Manufacturers / labelers
- 6
- Strengths listed
- 500 mg/1
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 8698
Drugs@FDA applications
Linked only where the FDA listing’s application number matches Drugs@FDA exactly. A listing in the NDC Directory does not by itself mean FDA approval.
| Application | Sponsor | Original approval | Listings |
|---|---|---|---|
| ANDA 080966 | LANNETT | 1976-07-29 | 3 |
| ANDA 084442 | WATSON LABS TEVA | 1977-03-02 | 1 |
| ANDA 217020 | RISING | 2023-11-20 | 3 |
Official labeling on DailyMed
- PROBENECID TABLET [REMEDYREPACK INC.] · version 1 · 2026-04-30
- PROBENECID TABLET [RISING PHARMA HOLDINGS, INC.] · version 5 · 2026-01-30
- PROBENECID TABLET, FILM COATED [MARLEX PHARMACEUTICALS INC] · version 11 · 2025-11-19
- PROBENECID TABLET, FILM COATED [ACTAVIS PHARMA, INC.] · version 13 · 2025-05-09
- PROBENECID TABLET [BRYANT RANCH PREPACK] · version 100 · 2024-08-16
- PROBENECID TABLET, FILM COATED [LANNETT COMPANY, INC.] · version 9 · 2024-07-04
- PROBENECID TABLET, FILM COATED [BRYANT RANCH PREPACK] · version 100 · 2024-01-29
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.