- New
Nest in Tub ISO 2R amber open sterile vials, 16x35mm, 100 vials.
3rd party sterility and endotoxin testing is performed by a USA accredited laboratory.
No minimum purchase and worldwide delivery.
Catalog VA1002NC105
We do not sell customer sales data.
Orders are generally shipped within 1 business day after receipt of payment, Monday through Friday.
Sterile items cannot be returned. All other items must receive a return authorization in writing.
Formulated for laboratories and compounding pharmacies that demand consistency, these 2R amber sterile vials are manufactured from USP Type I borosilicate glass for superior chemical resistance and protection against light-sensitive degradation.
Each vial measures 16mm x 35mm, matching standard ISO 2R specifications for precise fill-volume and closure compatibility.
Nested Tray in Tub Packaging — Built for Safe Transit: Every vial ships in a protection nested sleeve tray (comparable to a nested tray-in-tub format), holding 100 vials per tray. Individual cavities keep glass-to-glass contact to zero during shipping and handling, virtually eliminating chips, scuffs, and cosmetic damage before the vials ever reach your bench.
Refer to the product images for a full view of the tray design.
Right-Sized for Small-Batch Compounding - A 100-count tray is intentionally sized for smaller production runs, making these vials a practical fit for USP <797> compliance in Compounded Sterile Preparation (CSP) workflows — specifically batches requiring sterility testing at a final yield of 250 units or fewer. Order only what a given batch calls for, without breaking sterility assurance on a larger, unused case.
Sourced From a DMF-Registered Manufacturer - These vials are produced by a manufacturer holding an active Drug Master File (DMF) registration with the FDA, supporting regulatory traceability for pharmaceutical and compounding applications.
Full Quality Documentation Included - Each lot ships with complete third-party testing documentation: Sterility Testing and Endotoxin Testing report is performed by an independent, FDA-registered U.S. laboratory holding GMP, GLP, and GTP certifications, with ISO/IEC 17025 accreditation — giving you an added layer of quality assurance for regulated compounding and lab use.
Specific References
You might also like