ANDA 77467, held by Teva Pharms. Nateglinide.
As of Nov 15, 2026, ANDA 77467 (Nateglinide), held by Teva Pharms, was not approved, with 0 approved supplements and 0 published complete response letters.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Apr 26, 2007 | Original application | Tentative approval |
| Nateglinide60MG · tablet;oral | Nateglinide | Discontinued |
| Nateglinide120MG · tablet;oral | Nateglinide | Discontinued |
Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed daily; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters. Drugs@FDA and FDA complete response letters