Drug factory · FDA FEI 3002986480

International Vitamin Corporation

Anderson, South Carolina, United States

Matched to FDA's records by company name, because this plant's registration on the label has expired.

United States: 1

No problems found at FDA's last inspection, Mar 4, 2011.

No Action Indicated: inspectors found no objectionable conditions.

2 drug inspections on record since 2010: 2 with no problems, 0 with problems fixed voluntarily, 0 with FDA action.

What it does, for whom

DrugRoleForNDC
DutasterideMakes it Intergel Pharmaceuticals Inc 62112-8068
Folic Acid, Cholecalciferol, Pyridoxine Hydrochloride, Cyanocobalamin, Omega-3 FMakes it PBM Pharmaceuticals Inc. 66213-543
NifedipineMakes it, tests it and repackages it Intergel Pharmaceuticals Inc, Lupin Pharmaceuticals, Inc. 62112-8045, 43386-440

FDA inspection history

EndedResultProgramProblems noted
Mar 4, 2011No problems foundDrug Quality Assurance—
Jul 26, 2010No problems foundDrug Quality Assurance—