Clear  borosilicate glass serum vials (USP / ASTM Type I, Class A).
Sealed with gray butyl stopper and open center aluminum seal.
Vials contain no liquid.

Sterile and free of endotoxins.
Certificate of Analysis available upon request with your order.

Assembled units meet FDA mandated 14-day
sterility testing protocol.

Ideal for compounding pharmacies, veterinarians, etc.

            Processed and assembled by     

Not available unassembled.
Not available in amber glass.

Overview of Processing Procedures:

All processes are carried out under strict Class 100 U.S. Pharmacopoeia and Federal Code of Regulations methodologies.

1. Vials are washed with deionized water to removed any particulate matter, rinsed with Water for Injection @ 70^oC and blasted with cleaned compressed air to remove residual moisture.

2. Vials are placed in stainless steel pans and sterilized in dry heat for 5 hours @ 200^oC.  This accomplishes the sterilization and depyrogenation process.

3. Closures (stoppers) are steam sterilized @ 121^oC for 30 minutes, then dried for 2 to 8 hours @105^oF.

4. Vials and closures are then mechanically assembled in a Class 100 vial and diluent production room.

5. Each lot is held in quarantine for 14 days at which time samples are tested by an independent laboratory for sterility and endotoxins.  Once passed, the lot is released for sale.