single-dose vial


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single-dose vial

A container that holds enough medication for one patient's immediate needs. Single-dose vials should not be reused or refilled.
See also: vial
References in periodicals archive ?
This clinic routinely reused these single-dose vials for multiple patients, which established a pathway for the spread of HCV from one patient to another.
For patients with certain sensitivities, for whom the use of Wedgewood Pharmacy's regular formulation of 17P is contraindicated, the company also will provide a preservative-free 17-alpha hydroxyprogesterone caproate, 250mg/ml, in single-dose vials.
Food and Drug Administration (FDA) of its Abbreviated New Drug Application (ANDA) for Ondansetron Injection, USP, 2 mg/mL, Single-Dose Vials.
It is available in three presentations: 20mg/ml in single-dose vials, and 80 mg/4 mL or 160 mg/8 mL in multiple-dose vials.
In response to concerns over mercury toxicity in infants, vaccine manufacturers have worked to remove thimerosal by substituting other vaccine preservatives or moving to single-dose vials that don't require preservatives.
Aurobindo Pharma has gained final approval from the US Food & Drug Administration (US FDA) to produce and market Acetylcysteine injection, 6g/30 mL (200 mg/mL) single-dose vials.
Despite general support for the direction of the proposed legislation, NACDS provided an example showing that its definition of "compounding manufacturer" may inadvertently group into this category those pharmacies that repackage a drug using sterile preservative-free single-dose vials or by pooling sterile drugs.
The single-dose vials can be provided to the patient for in-home use.
Akorn-Strides, LLC today announced the approvals of two ANDAs for Famotidine Injection USP, 20 mg/2mL Single-Dose Vials and 40 mg/4mL & 200 mg/20mL Multiple-Dose Vials.
The approval will see the company manufacturing and marketing will approved Isosulfan Blue Injection 1% (50 mg/5 mL) single-dose vials and will introduce the product in the Q4 of FY15-16.
Its Bioniche Pharma unit was given FDA approval of its ANDA for fludarabine phosphate injection USR 25 mg/mL, packaged in 50 mg/2 mL single-dose vials.
Food and Drug Administration (FDA) has granted final approval for the Company's Abbreviated New Drug Applications (ANDA) to market its generic version of Roche's antinauseant and antiemetic agent Kytril([R]) (Granisetron Hydrochloride) Injection, 1 mg (base)/mL in 1 mL single-dose vials and 1 mg (base) Tablets.

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