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DEPO-PROVERA® CI Principal Display Panel (medroxyprogesterone acetate injectable suspension, for intramuscular use)

PRINCIPAL DISPLAY PANEL - 150 mg/mL Vial Label

NDC 0009-0746-30
Rx only

Depo-Provera®
Contraceptive
Injection

medroxyPROGESTERone acetate
injectable suspension, USP

150 mg/mL

PRINCIPAL DISPLAY PANEL - 150 mg/mL Vial Label

PRINCIPAL DISPLAY PANEL - 150 mg/mL Vial Carton

Pfizer

NDC 0009-0746-30
Rx only

Depo-Provera®
Contraceptive
Injection

medroxyPROGESTERone
acetate injectable
suspension, USP

150 mg/mL

1 mL Single-Dose Vial

For intramuscular use only

PRINCIPAL DISPLAY PANEL - 150 mg/mL Vial Carton

PRINCIPAL DISPLAY PANEL - 1 mL Syringe Label

Pfizer
NDC 0009-7376-11
Rx only

Depo-Provera®
Contraceptive Injection

150 mg per mL

medroxyprogesterone acetate
injectable suspension, USP

Intramuscular use only
1 mL Single Dose Syringe
Shake vigorously before use
Pfizer Inc, NY, NY 10017
819 361 101

LOT/EXP:

8Q2671

Principal Display Panel - 1 mL Syringe Label

PRINCIPAL DISPLAY PANEL - 1 mL Syringe Carton - NDC 0009-7376-11

NDC 0009-7376-11

Pfizer
Depo-Provera® Contraceptive Injection
(medroxyprogesterone acetate) injectable suspension, USP

150 mg per mL

Intramuscular use only
Single Use Syringe
Rx only

1 mL Prefilled Syringe

PRINCIPAL DISPLAY PANEL - 1 mL Syringe Carton - NDC 0009-7376-11
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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.