Sold as Keftab. Every FDA application for this active ingredient.
As of Nov 15, 2026, FDA lists 1 application for Cephalexin Hydrochloride (sold as Keftab), first approved Oct 29, 1987, with 0 new uses approved and 0 published complete response letters.
| Effects of Hypoxia or Caffeine on 4km Time-trial Morning Cycling.Caffeine, Hypoxia · Liverpool John Moores University | Phase 4 | Recruiting | Nov 13, 2026 |
| Precision Management of Urinary Tract Symptoms in Older WomenUrinary Tract Infection (Diagnosis) · Megan Bradley | Phase 3 | Recruiting | Jul 7, 2026 |
| Naproxen Versus Placebo as Adjunct Treatment of CellulitisCellulitis, Skin Disease, Infectious · Ottawa Hospital Research Institute | Phase 3 | Not yet recruiting | Jun 24, 2026 |
| Self-Start Triage Model for Post-Botox® Lower Urinary Tract SymptomsOveractive Bladder · The Cleveland Clinic | Early phase 1 | Recruiting | Jun 15, 2026 |
| Extended Oral Antibiotic Prophylaxis in Diabetic Fracture PatientsFracture Lower Leg, Diabetes · Texas Tech University Health Sciences Center, El Paso | Phase 4 | Recruiting | May 1, 2026 |
| Prophylactic Antibiotics for Outpatient Urethral BulkingUrinary Tract Infections, Stress Urinary Incontinence · University of Miami | Phase 4 | Recruiting | Mar 30, 2026 |
| Benson Relaxation Technique Effectiveness on Pain and Quality of Life Post Reconstructive MammoplastyBreast Cancer · Cairo University | Not applicable | Not yet recruiting | Jun 24, 2025 |
| A Platform Trial for Gram Negative Bloodstream InfectionsGram-negative Bacteremia · Sunnybrook Health Sciences Centre | Not applicable | Recruiting | Aug 5, 2024 |
Applications, approvals and products come from FDA's Drugs@FDA data files, refreshed weekly, grouped by active ingredient as FDA spells it. Complete response letters are FDA's published letters. Medicare spending is CMS's Part D and Part B dashboard, matched to this ingredient by generic name; shortages are FDA's shortage list, matched by application number; clinical trials are ClinicalTrials.gov studies naming the ingredient as an intervention, refreshed daily; safety programs are FDA's REMS list, matched by application number or, for shared programs, by ingredient. Drugs@FDA