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CAVERJECT® IMPULSE Principal Display Panel (alprostadil)

PRINCIPAL DISPLAY PANEL - 10 microgram Syringe Label

Caverject Impulse®

Dual Chamber System
alprostadil for injection

10 micrograms

KEEP OUT OF REACH OF CHILDREN

Pharmacia & Upjohn Co
DIVISION OF PFIZER INC, NY, NY 10017
MADE IN BELGIUM

8Q3129

LOT/EXP

Principal Display Panel - 10 microgram Syringe Label

PRINCIPAL DISPLAY PANEL - 10 micrograms Syringe Carton

Pfizer

Caverject Impulse®
alprostadil for injection

10 micrograms

NDC 0009-5181-01
Contains 2 of NDC 0009-5181-10

For intracavernosal use only
Dual Chamber System

Contains 2 single dose injection systems
Diluent Contains Benzyl Alcohol

Rx only

Principal Display Panel - 10 micrograms Syringe Carton

PRINCIPAL DISPLAY PANEL - 20 microgram Syringe Label

Caverject Impulse®

Dual Chamber System
alprostadil for injection

20 micrograms

KEEP OUT OF REACH OF CHILDREN

Pharmacia & Upjohn Co
DIVISION OF PFIZER INC, NY, NY 10017
MADE IN BELGIUM

8Q3130

LOT/EXP

Principal Display Panel - 20 microgram Syringe Label

PRINCIPAL DISPLAY PANEL - 20 micrograms Syringe Carton

Pfizer

Caverject Impulse®
alprostadil for injection

20 micrograms

NDC 0009-5182-01
Contains 2 of NDC 0009-5182-11

For intracavernosal use only
Dual Chamber System

Contains 2 single dose injection systems
Diluent Contains Benzyl Alcohol

Rx only

Principal Display Panel - 20 micrograms Syringe Carton
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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:

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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.