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DEPO-MEDROL® Single-dose Vial Principal Display Panel (methylprednisolone acetate injectable suspension, USP)

PRINCIPAL DISPLAY PANEL - 40 mg/mL Vial Label

NDC 0009-3073-01

1 mL Single-Dose Vial
Depo-Medrol®

(methylPREDNISolone
acetate injectable
suspension, USP)

40 mg/mL

Rx only

PRINCIPAL DISPLAY PANEL - 40 mg/mL Vial Label

PRINCIPAL DISPLAY PANEL - 40 mg/mL Vial Carton

NDC 0009-3073-03
Contains 25 of NDC 0009-3073-01

25—1 mL Single-Dose Vials
Depo-Medrol®

(methylPREDNISolone acetate
injectable suspension, USP)

40 mg/mL

For intramuscular, intrasynovial and soft tissue injection only
NOT for IV use

Pfizer Injectables

Rx only

PRINCIPAL DISPLAY PANEL - 40 mg/mL Vial Carton

PRINCIPAL DISPLAY PANEL - 80 mg/mL Vial Label

NDC 0009-3475-01

1 mL Single-Dose Vial
Depo-Medrol®

(methylPREDNISolone
acetate injectable
suspension, USP)

80 mg/mL

Rx only

PRINCIPAL DISPLAY PANEL - 80 mg/mL Vial Label

PRINCIPAL DISPLAY PANEL - 80 mg/mL Vial Carton

NDC 0009-3475-03
Contains 25 of NDC 0009-3475-01

25—1 mL Single-Dose Vials
Depo-Medrol®

(methylPREDNISolone acetate
injectable suspension, USP)

80 mg/mL

For intramuscular, intrasynovial and soft tissue injection only
NOT for IV use

Pfizer Injectables

Rx only

PRINCIPAL DISPLAY PANEL - 80 mg/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.