Molecules / Elvitegravir

Elvitegravir API manufacturers

CAS 697761-98-1 ATC J05AX11 Updated 9 July 2026
5
manufacturers with an active filing 5 of them hold a US DMF or a CEP
37
finished-dose makers across 17 regulators
Showing 5 of 5 manufacturers This list is ranked on evidence. Placement cannot be purchased.

Ranked API manufacturers

01

Gilead Sciences

United States
Makes the APIFinished dose
Credentials confirmed against the regulator files on 25 July 2026

Holds one active US DMF for elvitegravir, filing since 2011. Its 2026 FDA inspection closed as VAI, and its GMP is recognised in 47 markets.

US DMF
1 active
CEP
None on file
Last FDA inspection
2026 · VAI
GMP recognised in
47 markets
How this listing is sourced FDA, List of Drug Master Files
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02

Alembic Pharmaceuticals

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

Holds one active US DMF for elvitegravir, filing since 2020. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 18 markets.

US DMF
1 active
CEP
None on file
Last FDA inspection
2025 · VAI
GMP recognised in
18 markets
How this listing is sourced FDA, List of Drug Master Files
View profile
03

MSN Laboratories

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

Holds 2 active US DMFs for elvitegravir, filing since 2016. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 4 markets.

US DMF
2 active
CEP
None on file
Last FDA inspection
2024 · VAI
GMP recognised in
4 markets
How this listing is sourced FDA, List of Drug Master Files
View profile
04
Credentials confirmed against the regulator files on 25 July 2026

Holds one active US DMF for elvitegravir, filing since 2017. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 1 market.

US DMF
1 active
CEP
None on file
Last FDA inspection
2023 · VAI
GMP recognised in
1 markets
How this listing is sourced FDA, List of Drug Master Files
View profile
05

Matrix Pharmacorp

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

Holds 2 active US DMFs for elvitegravir, filing since 2013. Its 2025 FDA inspection closed as VAI.

US DMF
2 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
View profile

2 more manufacturers hold filings for elvitegravir

The names are listed below. Ask Fred about the filings, inspection history and GMP certificates on record for each manufacturer.

Shanghai Desano Chemical PharmaceuticalMatrix Pharmacorp
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Finished-dose makers (5)

Zentiva, k.s Czech Republic Sandoz Switzerland Zydus Lifesciences India Patheon Canada Krka Slovenia

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

Who makes elvitegravir?

Ask Fred which manufacturers are on record for elvitegravir and what filings they hold.

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Also on this molecule

Finished dose 5 Contract mfrs 0