ANDA 219175, held by Lupin. Phytonadione.
As of Nov 15, 2026, ANDA 219175 (Phytonadione), held by Lupin, was first approved by FDA on Sep 30, 2026, with 0 approved supplements and 0 published complete response letters.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Sep 30, 2026 | Original application | Approved | None posted |
| Product | Active ingredient | Marketing |
|---|---|---|
| Phytonadione1MG/0.5ML ยท injectable;injection | Phytonadione | Rx |
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
