NDAORALTABLET, CHEWABLE
Approved
Aug 1970
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Data completeness
3/8 — Basic
ERYPED (erythromycin ethylsuccinate) by R-Pharm US is clinical pharmacology orally administered erythromycin ethylsuccinate suspension is readily and reliably absorbed under both fasting and nonfasting conditions. Approved for the following infections caused by chlamydia trachomatis : conjunctivitis of the newborn, pneumonia of infancy, urogenital infections during pregnancy and 8 more indications. First approved in 1970.
Drug data last refreshed Yesterday · AI intelligence enriched 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
ERYPED (erythromycin ethylsuccinate) is an oral macrolide antibiotic indicated for bacterial and chlamydial infections, including newborn conjunctivitis, pneumonia of infancy, and urogenital infections. It works by inhibiting protein synthesis via 50S ribosomal subunit binding in susceptible organisms. The drug is readily absorbed orally and concentrates in the liver for biliary excretion.
LOE Approaching
Lifecycle stage indicates mature product with limited commercial expansion; team size likely stable to declining as patent LOE approaches.
Mechanism of Action
CLINICAL PHARMACOLOGY Orally administered erythromycin ethylsuccinate suspension is readily and reliably absorbed under both fasting and nonfasting conditions. Erythromycin diffuses readily into most body fluids. Only low concentrations are normally achieved in the spinal fluid, but passage of the…
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.