Class II · Moderate risk
Depo-Medrol
cGMP deviations: Temperature abuse
National Drug Code
Is NDC 0009-3073-23 recalled?
Depo-Medrol · 25 VIAL, SINGLE-DOSE in 1 PACKAGE (0009-3073-23) / 1 mL in 1 VIAL, SINGLE-DOSE
Yes — this exact package was recalled
1 FDA recall names the code 0009-3073-23 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- methylprednisolone acetate
- Strength
- METHYLPREDNISOLONE ACETATE 40 mg/mL
- Form
- Injection, Suspension · Intralesional, Intramuscular, Intrasynovial, Soft Tissue
- Labeler
- Pharmacia & Upjohn Company LLC
- Type
- Human Prescription Drug
- Product code
- 0009-3073
Recalls naming this package
Class III · Low risk
Depo-Medrol
Failed pH Specification: A pH result of 2.9 was obtained at the 9 month stability test interval at 25C/60%RH. The registered specification for pH is 3.0 - 7.0
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
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