ANDA 86968, held by Lederle. Prednisone.
As of Nov 14, 2026, ANDA 86968 (Prednisone), held by Lederle, was not approved, with 2 approved supplements and 0 published complete response letters.
| Product | Active ingredient | Marketing |
|---|---|---|
| Prednisone5MG ยท tablet;oral | Prednisone | Discontinued |
| Jul 24, 1984 | Supplement 2Manufacturing | Approved | None posted |
| Jul 27, 1982 | Supplement 1Manufacturing | Approved | None posted |
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