Prescribing Information
Download Prescribing Information

Health Professional Information

How Supplied/Storage and Handling

HOW SUPPLIED

Atracurium Besylate Injection USP, each mL containing 10 mg atracurium besylate, is supplied as follows:

Unit of SaleConcentration
*
Contains benzyl alcohol (see WARNINGS).
NDC 0409-1109-01
Carton of 10 Single dose Vials
50 mg/5 mL
(10 mg/mL)
NDC 0409-1105-02
*Carton of 10 Multiple dose Vials
100 mg/10 mL
(10 mg/mL)

Atracurium Besylate Injection should be refrigerated at 2°C to 8°C (36°F to 46°F) to preserve potency. DO NOT FREEZE. Protect from light. Keep vials in carton until time of use.

Upon removal from refrigeration to room temperature storage conditions (25°C/77°F), use Atracurium Besylate Injection within 14 days even if rerefrigerated.

 

Manufactured by:

Gland Pharma Limited;

Hyderabad 500043, India

 

Logo

Manufactured for:

Hospira, Inc.

Lake Forest, IL 60045 USA

 

 

LAB-1214-4.0
Revised: 07/2021

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.