Prestige Packaging is an FDA regulated facility and has been audited by the FDA numerous times with no 483s ever issued requiring any action by Prestige.
Prestige Packaging conforms to the U.S. Food and Drug Administration’s Code of Federal Regulations (CFR) 21 Parts 210 and 211, current Good Manufacturing Practices (cGMP) and to the quality system standards of the Quality System Regulation for OTC drug Products CFR Part 328.
- FEI (Facility Establishment Identifier) #1833338
- DUNS #170837962
- Florida OTC License #21758
Prestige also performs secondary packaging of the unit dose packets into the cartons and follows CFR Part 201 for drug facts labeling.
Prestige Packaging, including its management, employees, consultants and other advisors, is committed to providing high-quality products fully fit for their intended use by our customers.
Our Quality Policies reflect the commitment to meeting or exceeding customer expectations through continuous improvement, the adoption and implementation of relevant quality standards, and recognition that the patient is the ultimate customer.