NDA 50219, held by Lilly. Cephaloglycin.
As of Nov 13, 2026, NDA 50219 (Kafocin), held by Lilly, was first approved by FDA on Jun 12, 1970, with 0 approved supplements and 0 published complete response letters.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Jun 12, 1970 | Original application | Approved | None posted |
| Product | Active ingredient | Marketing |
|---|---|---|
| Kafocin250MG ยท capsule;oral | Cephaloglycin | 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