Drug factory · FDA FEI 3004611182
Apitoria Pharma Private Limited
Unit-IV, Sy.No's.52, 53, 58, 59, 61 to 78, 127&128, Pydibhimavaram V & Sy.No 1, 2, 4to9, 11, 29, 30, 31&32, Chittivalasa V, Ranasthalam Mandal, Srikakulam, India
No problems found at FDA's last inspection, Sep 11, 2026.
No Action Indicated: inspectors found no objectionable conditions.
7 drug inspections on record since 2009: 4 with no problems, 2 with problems fixed voluntarily, 1 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Ibandronic Acid | Makes the active ingredient and tests it | AuroMedics Pharma LLC | 55150-191 |
| Levetiracetam | Makes the active ingredient | IntelliPharmaCeutics Corp. | 35208-031, 35208-032 |
| Levofloxacin | Makes the active ingredient and tests it | AuroMedics Pharma LLC | 55150-156, 55150-157 |
| Sildenafil | Makes the active ingredient and tests it | AuroMedics Pharma LLC | 55150-166 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Sep 11, 2026 | No problems found | Drug Quality Assurance | — |
| Aug 2, 2022 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Feb 9, 2019 | Serious problems, FDA action | Drug Quality Assurance | — |
| Feb 21, 2017 | No problems found | Drug Quality Assurance | — |
| Apr 30, 2015 | No problems found | Drug Quality Assurance | — |
| Jun 8, 2012 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Oct 22, 2009 | No problems found | Drug Quality Assurance | — |
Registered with FDA for: analysis; api manufacture.