Molecules / Ganciclovir

Ganciclovir API manufacturers

CAS 82410-32-0 ATC J05AB06 · Nucleoside antivirals Updated 9 July 2026
8
manufacturers with an active filing 4 of them hold a US DMF or a CEP
34
shortage records on file across 8 countries
180
finished-dose makers across 40 regulators
Showing 8 of 8 manufacturers This list is ranked on evidence. Placement cannot be purchased.

Ranked API manufacturers

01

Excella Gmbh

Germany
Makes the API
Credentials confirmed against the regulator files on 25 July 2026

Holds 2 active US DMFs and one valid CEP for ganciclovir, filing since 2001. Its 2022 FDA inspection closed as VAI, and its GMP is recognised in 7 markets.

US DMF
2 active
CEP
1 valid
Last FDA inspection
2022 · VAI
GMP recognised in
7 markets
03

Apitoria Pharma

India
Makes the API
Credentials confirmed against the regulator files on 25 July 2026

Holds one active US DMF for ganciclovir, filing since 2017. Its 2025 FDA inspection closed as VAI.

US DMF
1 active
CEP
None on file
Last FDA inspection
2025 · VAI
GMP recognised in
Not established
How this listing is sourced FDA, List of Drug Master Files
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04

Trifarma

Italy
Makes the API
Credentials confirmed against the regulator files on 25 July 2026

Holds one active US DMF for ganciclovir, filing since 2010. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 1 market.

US DMF
1 active
CEP
None on file
Last FDA inspection
2024 · VAI
GMP recognised in
1 markets
How this listing is sourced FDA, List of Drug Master Files
View profile
05

Hainan Poly Pharm

China
Makes the APIFinished dose

Registered with SFDA (Saudi Arabia) for ganciclovir. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 6 markets.

US DMF
None on file
CEP
None on file
Last FDA inspection
2023 · VAI
GMP recognised in
6 markets
How this listing is sourced Regulator filings, warehouse snapshot 9 July 2026
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06

Corden Pharma

United States
Makes the API

Registered with SFDA (Saudi Arabia) for ganciclovir.

US DMF
None on file
CEP
None on file
Last FDA inspection
Not established
GMP recognised in
Not established
How this listing is sourced Regulator filings, warehouse snapshot 9 July 2026
View profile
07

Công ty cổ phần Dược phẩm An Thiên

Vietnam
Makes the APIFinished dose

Registered with DAV (Vietnam) for ganciclovir. Its GMP is recognised in 1 market.

US DMF
None on file
CEP
None on file
Last FDA inspection
Not established
GMP recognised in
1 markets
How this listing is sourced Regulator filings, warehouse snapshot 9 July 2026
View profile
08

Registered with SFDA (Saudi Arabia) for ganciclovir. Its 2025 FDA inspection closed as OAI, and its GMP is recognised in 2 markets.

US DMF
None on file
CEP
None on file
Last FDA inspection
2025 · OAI
GMP recognised in
2 markets
How this listing is sourced Regulator filings, warehouse snapshot 9 July 2026
View profile

5 more manufacturers hold filings for ganciclovir

The names are listed below. The filings, inspection history and GMP certificates behind each one are available with a free account.

Open the full list with a free account

Contract manufacturers (8)

How this list is built

The order is set by active filings weighted by regulator, inspection outcomes and their recency, breadth of GMP recognition, and evidence of real exports, less any open risk flags. Every factor appears on the card it produced. Read the full method.

Active US DMFs
FDA, List of Drug Master Files
Valid CEPs
EDQM certificate database
Inspection outcomes
FDA inspection classifications
GMP certificates
EudraGMDP and national regulators

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