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ELLENCE®Principal Display Panel (epirubicin HCl)

PRINCIPAL DISPLAY PANEL - 50 mg/25 mL Vial Label

NDC 0009-5091-01
Rx only

Single-dose Vial
Ellence®
epirubicin hydrochloride
injection

50 mg/25 mL
(2 mg/mL)

For Intravenous Use Only

PRINCIPAL DISPLAY PANEL - 50 mg/25 mL Vial Label

PRINCIPAL DISPLAY PANEL - 50 mg/25 mL Vial Carton

NDC 0009-5091-01
Rx only

Single-dose Vial
Ellence®
epirubicin hydrochloride
injection

50 mg/25 mL
(2 mg/mL)

For Intravenous Use Only

Pfizer Injectables

PRINCIPAL DISPLAY PANEL - 50 mg/25 mL Vial Carton

PRINCIPAL DISPLAY PANEL - 200 mg/100 mL Vial Label

NDC 0009-5093-01
Rx only

Single-dose Vial
Ellence®
epirubicin hydrochloride
injection
200 mg/100 mL
(2 mg/mL)

For Intravenous Use Only

Pfizer Injectables

PRINCIPAL DISPLAY PANEL - 200 mg/100 mL Vial Label

PRINCIPAL DISPLAY PANEL - 200 mg/100 mL Vial Carton

NDC 0009-5093-01
Rx only

Single-dose Vial
Ellence®
epirubicin hydrochloride
injection

200 mg/100 mL
(2 mg/mL)

For Intravenous Use Only

Pfizer Injectables

PRINCIPAL DISPLAY PANEL - 200 mg/100 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.