(Dextrose 50% LifeShield® Abboject®, Abboject®, Ansyr® Syringe)

Prescribing Information
Download Prescribing Information

Health Professional Information

How Supplied/Storage and Handling

HOW SUPPLIED

50% Dextrose Injection, USP is supplied in single-dose containers as follows:

Unit of Sale and Product DescriptionStrength
(Concentration)
NDC

Bundle of 10
50 mL LifeShield® Abboject® Unit of Use Syringe with Male Luer Lock adapter and protected needle

25 g/50 mL
(0.5 g/mL)

0409-4902-34

Bundle of 10
50 mL Single-Dose Abboject® Syringe with Male Luer Lock Adapter

25 g/50 mL
(0.5 g/mL)

0409-0505-25

Tray of 25
50 mL Single-Dose Fliptop Vials

25 g/50 mL
(0.5 g/mL)

0409-6648-02

Bundle of 10
50 mL Ansyr® II Plastic Syringe with syringe and barrel detached

25 g/50 mL
(0.5 g/mL)

0409-7517-16

Exposure of pharmaceutical products to heat should be minimized. Avoid excessive heat. Protect from freezing. Store at 20 to 25°C (68 to 77°F). [See USP Controlled Room Temperature.]

Medication Guide
Download Consumer Medicine Information

Health Professional Information

{{section_name_patient}}

{{section_body_html_patient}}

Additional Resources

Chat online with Pfizer Medical Information regarding your inquiry on a Pfizer medicine or vaccine.

Speak with a Pfizer Medical Information Professional regarding your Pfizer medicine or vaccine inquiry.

Available 9AM-5PM ET Monday to Friday; excluding holidays.

 

Submit a medical question for a Pfizer medicine or a vaccine. 

The submission will be reviewed during our standard business hours.

To report an adverse event related to a Pfizer product and you are not part of a clinical trial* for this medication, click the link below to submit your information: 
Pfizer Safety Reporting Site

*If you are involved in a clinical trial for either product, adverse events should be reported to your coordinating study site.

If you cannot use the above website to report an adverse event related to a Pfizer medication, please call (800) 438-1985.

You may also contact the U.S. Food and Drug Administration (FDA) directly to report adverse events or product quality concerns either online at www.fda.gov/medwatch or by calling (800) 332-1088.