It allows for drug admixture after connection to a .
A breakaway seal in the tube between the vial adaptor and the container is broken to allow transfer of the diluent into the vial and reconstitution of the drug.
Expiration Dates Expiration dates are assigned by the manufacturer of a product and indicate when a product has lost sufficient strength that it is outside acceptable limits established for the product.
At this point, that product should not be dispensed or used.
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They would be assembled in a hood (ISO 5), and the medication does not require refrigeration.
However, biological testing was supportive of the safety of the plastic container materials.
A question was brought up about what the BUD of an assembled, but not activated Minibag-Plus system would be.
Plus Container is a sterile, nonpyrogenic solution for intravenous administration after admixture with a single dose powdered drug. Each 100 m L contains 900 mg of Sodium Chloride, USP (Na Cl). The reconstituted drug is then transferred from the vial into the container diluent and mixed to result in an admixture for delivery to the patient. Exposure to temperatures above 25°C/77°F during transport and storage will lead to minor losses in moisture content. It is unlikely that these minor losses will lead to clinically significant changes within the expiration period.
It contains 154 m Eq/L of sodium and 154 m Eq/L of chloride. A breakaway seal in the tube between the vial adaptor and the container is broken to allow transfer of the diluent into the vial and reconstitution of the drug.