NDA 50550, held by Lilly. Moxalactam Disodium.
As of Nov 13, 2026, NDA 50550 (Moxam), held by Lilly, was not approved, with 0 approved supplements and 0 published complete response letters.
| Product | Active ingredient | Marketing |
|---|---|---|
| MoxamEQ 250MG BASE/VIAL · injectable;injection | Moxalactam Disodium | Discontinued |
| MoxamEQ 500MG BASE/VIAL · injectable;injection | Moxalactam Disodium | Discontinued |
| MoxamEQ 1GM BASE/VIAL · injectable;injection | Moxalactam Disodium | Discontinued |
| MoxamEQ 2GM BASE/VIAL · injectable;injection | Moxalactam Disodium | Discontinued |
| MoxamEQ 10GM BASE/VIAL · injectable;injection | Moxalactam Disodium | 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