NDAORALTABLET
Approved
Nov 1951
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Clinical Trials
1
Data completeness
4/8 — Partial
CORTISONE ACETATE (cortisone acetate) by Pfizer is clinical pharmacology: naturally occurring glucocorticoids (hydrocortisone and cortisone), which also have salt-retaining properties, are used as replacement therapy in adrenocortical deficiency states. Approved for prostate cancer, atopic dermatitis, chronic kidney disease and 1 more indications. First approved in 1951.
Drug data last refreshed 21h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
Cortisone acetate is a naturally occurring glucocorticoid used for replacement therapy in adrenocortical deficiency and as a potent anti-inflammatory agent across multiple organ systems. It modifies immune responses and produces profound metabolic effects, making it a foundational corticosteroid therapy. The oral tablet formulation has been a clinical staple since 1951.
LOE Approaching
As a legacy product approaching LOE with minimal competitive pressure (30%), the brand team is likely focused on cost optimization and portfolio integration rather than growth initiatives.
Mechanism of Action
CLINICAL PHARMACOLOGY: Naturally occurring glucocorticoids (hydrocortisone and cortisone), which also have salt-retaining properties, are used as replacement therapy in adrenocortical deficiency states. They are also used for their potent anti-inflammatory effects in disorders of many organ…
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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.