General MedicationsORALStandard
ORLYNVAH
PROBENECID; SULOPENEM ETZADROXIL
Standard Dose
500MG;500MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Prescription
Summary
Approval overview ORLYNVAH is listed in Drugs@FDA under application 213972 (NDA).
Review priority: STANDARD Marketing status: Prescription Active ingredient PROBENECID; SULOPENEM ETZADROXIL Form and strength TABLET;ORAL - 500MG;500MG Sponsor ITERUM THERAP Submission history Latest submission status date: 2025-12-23 00:00:00.
Structured Monograph
Clinical summary
Approval overview ORLYNVAH is listed in Drugs@FDA under application 213972 (NDA). Review priority: STANDARD Marketing status: Prescription Active ingredient PROBENECID; SULOPENEM ETZADROXIL Form and strength TABLET;ORAL - 500MG;500MG Sponsor ITERUM THERAP Submission history Latest submission status date: 2025-12-23 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Prescription
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.