NORDITROPIN FLEXPRO (somatropin) by Novo Nordisk. Approved for recombinant human growth hormone [epc]. First approved in 2000.
Drug data last refreshed 8h ago · AI intelligence enriched 3w ago
NORDITROPIN FLEXPRO is a recombinant human growth hormone (somatropin) delivered via injection for treatment of growth hormone deficiency and related conditions. It is a biologic therapeutic that replaces or supplements endogenous growth hormone to promote growth, metabolism, and body composition. The product leverages Novo Nordisk's FlexPro pen delivery technology to enhance patient convenience and adherence.
Product is approaching loss of exclusivity with modest Part D spending of $11M in 2023; team size and hiring likely focused on transition and lifecycle extension strategies.
Recombinant Human Growth Hormone
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
The Efficacy and Safety of Inpegsomatropin Injection in Children With Turner Syndrome (TS) and Short Stature
Safety, Pharmacokinetic (PK) Profile and Efficacy of Inpegsomatropin Injection in Adults With Growth Hormone Deficiency
A Study to Learn How Different Injector Pens Affect the Study Medicine Called Genotropin (Somatropin) Delivery and Taken up Into the Blood in Healthy Adults
The Efficacy and Safety of Inpegsomatropin Injection in Children With Short Stature Born Small for Gestational Age
Trial Investigating the Efficacy and Safety of Weekly Lonapegsomatropin Compared to Daily Somatropin in Children and Adolescents With Short Stature or Growth Failure Due to Growth Hormone Sufficient Disorders
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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.
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Working on NORDITROPIN FLEXPRO offers limited but focused career opportunities in a late-lifecycle biologic product, primarily in clinical science and publication strategy roles. This assignment is best suited for professionals seeking stability in a mature therapeutic area rather than high-growth product exposure.
2 open roles linked to this drug