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

PRINCIPAL DISPLAY PANEL - 100 mg/5 mL Vial Label

5 mL Multidose Vial
NDC 0009-0274-01

Depo-Medrol®
(methylPREDNISolone acetate
injectable suspension, USP)

100 mg/5 mL

(20 mg/mL)
Rx only

PRINCIPAL DISPLAY PANEL - 100 mg/5 mL Vial Label

PRINCIPAL DISPLAY PANEL - 100 mg/5 mL Vial Carton

5 mL
Multidose Vial

NDC 0009-0274-01

Depo-Medrol®
(methylPREDNISolone
acetate injectable
suspension, USP)

100 mg/5 mL

(20 mg/mL)

For intramuscular,
intrasynovial and
soft tissue injection only

NOT for IV use

Contains Benzyl Alcohol
as a Preservative

Rx only

Pfizer Injectables

PRINCIPAL DISPLAY PANEL - 100 mg/5 mL Vial Carton

PRINCIPAL DISPLAY PANEL - 200 mg/5 mL Vial Label

5 mL Multidose Vial
NDC 0009-0280-02

Depo-Medrol®
(methylPREDNISolone acetate
injectable suspension, USP)

200 mg/5 mL
(40 mg/mL)

Rx only

PRINCIPAL DISPLAY PANEL - 200 mg/5 mL Vial Label

PRINCIPAL DISPLAY PANEL - 200 mg/5 mL Vial Package

25—5 mL Multidose Vials

NDC 0009-0280-51
Contains 25 of NDC 0009-0280-02

Depo-Medrol®
(methylPREDNISolone acetate injectable suspension, USP)

200 mg/5 mL
(40 mg/mL)

For intramuscular, intrasynovial and soft tissue injection only
NOT for IV use
Contains Benzyl Alcohol as a Preservative

Pfizer Injectables

Rx only

PRINCIPAL DISPLAY PANEL - 200 mg/5 mL Vial Package

PRINCIPAL DISPLAY PANEL - 400 mg/5 mL Vial Label

5 mL Multidose Vial
NDC 0009-0306-02

Depo-Medrol®
(methylPREDNISolone acetate
injectable suspension, USP)

400 mg/5 mL
(80 mg/mL)

Rx only

PRINCIPAL DISPLAY PANEL - 400 mg/5 mL Vial Label

PRINCIPAL DISPLAY PANEL - 400 mg/5 mL Vial Carton

5 mL
Multidose Vial

NDC 0009-0306-02

Depo-Medrol®
(methylPREDNISolone
acetate injectable
suspension, USP)

400 mg/5 mL
(80 mg/mL)

For intramuscular,
intrasynovial and
soft tissue injection only

NOT for IV use

Contains Benzyl Alcohol
as a Preservative

Rx only

Pfizer Injectables

PRINCIPAL DISPLAY PANEL - 400 mg/5 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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(800) 438-1985.
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.