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PROTONIX®Principal Display Panel (pantoprazole sodium)

PRINCIPAL DISPLAY PANEL - 20 mg Tablet Bottle Label

ALWAYS DISPENSE WITH
MEDICATION GUIDE

Pfizer
NDC 0008-0843-81

Protonix®
(pantoprazole sodium)
delayed-release tablets

20 mg

Swallow tablets whole. Do NOT
split, chew, or crush tablets.

90 Tablets
Rx only

Principal Display Panel - 20 mg Tablet Bottle Label

PRINCIPAL DISPLAY PANEL - 40 mg Tablet Bottle Label

ALWAYS DISPENSE WITH
MEDICATION GUIDE

Pfizer
NDC 0008-0841-81

Protonix®
(pantoprazole sodium)
delayed-release tablets

40 mg

Swallow tablets whole. Do NOT
split, chew, or crush tablets.

90 Tablets
Rx only

Principal Display Panel - 40 mg Tablet Bottle Label

PRINCIPAL DISPLAY PANEL - 40 mg Packet

NDC 0008-0844-01

Pfizer

Protonix®
40 mg
(pantoprazole sodium)

For Delayed-Release Oral Suspension*
*suspension in apple juice or applesauce only

Each packet contains:
Pantoprazole
40 mg
(equivalent to 45.1 mg of pantoprazole sodium)

14287101
F.2/0518/6103546
Code 40

Rx only

Principal Display Panel - 40 mg Packet

PRINCIPAL DISPLAY PANEL - 40 mg Packet Carton

Pfizer

NDC 0008-0844-02

ALWAYS DISPENSE WITH MEDICATION GUIDE

Protonix®
40 mg
(pantoprazole sodium)

For Delayed-Release Oral Suspension*
*suspension in apple juice or applesauce only

Rx only
30 Packets

Principal Display Panel - 40 mg Packet 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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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.