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ZIRABEV Principal Display Panel (bevacizumab-bvzr)

PRINCIPAL DISPLAY PANEL - 4 mL Vial Label

NDC 0069-0315-01
Rx only

Zirabev™
(bevacizumab–bvzr)
Injection

100 mg/4 mL
(25 mg/mL)

For Intravenous Infusion
After Dilution
One SINGLE-DOSE VIAL
DISCARD UNUSED PORTION.

PRINCIPAL DISPLAY PANEL - 4 mL Vial Label

PRINCIPAL DISPLAY PANEL - 4 mL Vial Carton

NDC 0069-0315-01

Zirabev™
(bevacizumab–bvzr)
Injection

100 mg/4 mL
(25 mg/mL)

For Intravenous Infusion
After Dilution

One SINGLE-DOSE VIAL

DISCARD UNUSED PORTION.

Rx only

Pfizer Oncology

PRINCIPAL DISPLAY PANEL - 4 mL Vial Carton

PRINCIPAL DISPLAY PANEL - 16 mL Vial Label

NDC 0069-0342-01
Rx only

Zirabev™
(bevacizumab–bvzr)
Injection

400 mg/16 mL
(25 mg/mL)

For Intravenous Infusion
After Dilution
One SINGLE-DOSE VIAL
DISCARD UNUSED PORTION.

PRINCIPAL DISPLAY PANEL - 16 mL Vial Label

PRINCIPAL DISPLAY PANEL - 16 mL Vial Carton

NDC 0069-0342-01

Zirabev™
(bevacizumab–bvzr)
Injection

400 mg/16 mL
(25 mg/mL)

For Intravenous Infusion
After Dilution

One SINGLE-DOSE VIAL

DISCARD UNUSED PORTION.

Rx only

Pfizer Oncology

PRINCIPAL DISPLAY PANEL - 16 mL Vial Carton
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Report Adverse Event
Pfizer Safety

To report an adverse event related to Pfizer-BioNTech COVID-19 Vaccine (also known as COMIRNATY®, COVID-19 mRNA, Vaccine BNT162b2 or BNT162) or Pfizer COVID-19 Treatment (also known as PAXLOVID™ (nirmatrelvir tablets; ritonavir tablets)), and you are not part of a clinical trial* for this product, 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.

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FDA Medwatch
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/medwatchor by calling
(800)-332-1088.