Reduces lipodystrophy. Sold as Egrifta. Every FDA application for this active ingredient.
As of Nov 15, 2026, FDA lists 1 application for Tesamorelin Acetate (sold as Egrifta), first approved Nov 10, 2010, with 0 new uses approved and 0 published complete response letters.
| Egrifta Sv | Part D | $42.4M | +14% | 782 |
| Egrifta Wr | Part D | $1.7M | New | 85 |
| Approved | Application | Sponsor | Supplements | Marketing |
|---|---|---|---|---|
| Nov 10, 2010 | EgriftaBLA 22505 ยท New molecular entity | Theratechnologies | 11 | Marketed |
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
