ANDA 62435, held by Glaxosmithkline. Cephalothin Sodium.
As of Nov 15, 2026, ANDA 62435 (Seffin), held by Glaxosmithkline, was not approved, with 0 approved supplements and 0 published complete response letters.
| SeffinEQ 1GM BASE/VIAL · injectable;injection | Cephalothin Sodium | Discontinued |
| SeffinEQ 2GM BASE/VIAL · injectable;injection | Cephalothin Sodium | Discontinued |
| SeffinEQ 10GM BASE/VIAL · injectable;injection | Cephalothin Sodium | 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