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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.

If you cannot use the above website or would like to report an adverse event related to a different Pfizer product, please call Pfizer Safety at
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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.