Class II ยท Moderate risk
MethylPREDNISolone Acetate Injectable Suspension
Presence of Particulate Matter: Potential for black particulates in the drug product.
National Drug Code
Is NDC 25021-0820-10 recalled?
methylprednisolone acetate · 1 VIAL in 1 CARTON (25021-820-10) / 10 mL in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 25021-0820-10 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.
1 of these recalls is still ongoing.
- Active ingredient
- methylprednisolone acetate
- Strength
- METHYLPREDNISOLONE ACETATE 40 mg/mL
- Form
- Injection, Suspension · Intra-Articular, Intralesional, Intramuscular, Intrasynovial, Soft Tissue
- Labeler
- Sagent Pharmaceuticals
- Type
- Human Prescription Drug
- Product code
- 25021-0820
Recalls naming this package
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
- 25021-0163 See recall 2
- 25021-0254 Docetaxel 2
- 25021-0701 Ketorolac Tromethamine 2
- 25021-0113 See recall 1
- 25021-0139 See recall 1
- 25021-0140 See recall 1
Free recall alerts
Know the day your medication is recalled
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