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Depo-Provera CI is supplied in the following strengths and package configurations:
| Package Configuration | Strength | NDC |
|---|---|---|
| Depo-Provera CI (medroxyprogesterone acetate sterile aqueous suspension 150 mg/mL) | ||
| 1 mL vial | 150 mg/mL | NDC 0009-0746-30 |
| 25 × 1 mL vials | 150 mg/mL | NDC 0009-0746-35 |
| Depo-Provera CI prefilled syringes packaged with 22 gauge × 1 1/2 inch Terumo® SurGuard™ Needles | ||
| 1 mL prefilled syringe | 150 mg/mL | NDC 0009-7376-11 |
To report an adverse event related to the Pfizer-BioNTech COVID-19 Vaccine, and you are not part of a clinical trial* for this product, click the link below to submit your information:
*If you are involved in a clinical trial for this 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 (800) 438-1985.
You may also contact the U.S. Food and Drug Administration (FDA) directly to report adverse events or product quality concerns either online at https://vaers.hhs.gov or call (800) 822-7967.
