Sold as Starlix. Every FDA application for this active ingredient: 1 branded and 8 generic.
As of Nov 15, 2026, FDA lists 9 applications for Nateglinide (sold as Starlix), first approved Dec 22, 2000, with 1 new use approved and 0 published complete response letters.
| Product | Part | Spending, 2025 | Change | Beneficiaries |
|---|---|---|---|---|
| Nateglinide | Part D | $7.3M | -12% | 37,232 |
| Dec 22, 2000 | StarlixNDA 21204 · New molecular entity | Novartis | 16 | Discontinued |
| Sep 9, 2009 | NateglinideANDA 77461 | Dr Reddys Labs Ltd | 4 | Marketed |
| Sep 9, 2009 | NateglinideANDA 77463 | Strides Pharma Intl | 5 | Marketed |
| Mar 30, 2011 | NateglinideANDA 77462 | Watson Labs | 3 | Marketed |
| Dec 11, 2015 | NateglinideANDA 205055 | Alvogen | 2 | Discontinued |
| Jul 6, 2016 | NateglinideANDA 205248 | Zydus Pharms | 3 | Marketed |
| Jun 18, 2018 | NateglinideANDA 205544 | Rising | 1 | Marketed |
| Apr 19, 2019 | NateglinideANDA 206432 | Cadila Pharms Ltd | 1 | Marketed |
| — | NateglinideANDA 77467 | Teva Pharms | 0 | Discontinued |
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