Drug factory · FDA FEI 3003227156
Matrix Pharmacorp Private Limited
Unit 7, Plot No. 14, 99 and 100, IDA, Pashamylaram Phase II, Patancheru, Sangareddy District, Hyderabad, India
Problems found, fixed voluntarily at FDA's last inspection, Nov 28, 2025.
Voluntary Action Indicated: inspectors found problems, but not serious enough for FDA to take action. The company is expected to fix them.
6 drug inspections on record since 2009: 1 with no problems, 5 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Desvenlafaxine | Makes the active ingredient | IntelliPharmaCeutics Corp. | 35208-009, 35208-010 |
| Hydrochlorothiazide and Lisinopril | Makes the active ingredient | Ranbaxy Laboratories Inc. | 63304-536, 63304-537, 63304-538 |
| Lisinopril | Makes the active ingredient | Ranbaxy Laboratories Inc. | 63304-531, 63304-532, 63304-533 +3 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Nov 28, 2025 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Sep 17, 2022 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Dec 30, 2016 | No problems found | Drug Quality Assurance | — |
| Aug 21, 2015 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Jun 21, 2012 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Apr 3, 2009 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
Registered with FDA for: analysis; api manufacture.