Treats acquired immunodeficiency syndrome (AIDS). ANDA 204204, held by Hainan Poly. Ganciclovir Sodium.
As of Nov 15, 2026, ANDA 204204 (Ganciclovir Sodium), held by Hainan Poly, was first approved by FDA on Nov 8, 2018, with 0 approved supplements and 0 published complete response letters.
Ganciclovir for Injection, USP is a deoxynucleoside analogue cytomegalovirus (CMV) DNA polymerase inhibitor indicated for the: Treatment of CMV retinitis in immunocompromised adult patients, including patients with acquired immunodeficiency syndrome (AIDS). Prevention of CMV disease in adult transplant recipients at risk for CMV disease. 1.1 Treatment of CMV Retinitis Ganciclovir for Injection, USP is indicated for the treatment of cytomegalovirus (CMV) retinitis in immunocompromised adult patients, including patients with acquired immunodeficiency syndrome (AIDS). 1.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Nov 8, 2018 | Original application | Approved | None posted |
| Product | Active ingredient | Marketing |
|---|---|---|
| Ganciclovir SodiumEQ 500MG BASE/VIAL · injectable;injection | Ganciclovir Sodium | 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
