NDC 0143-9850
Methylprednisolone Sodium Succinate 500 mg injection, powder, for solution
On the label: Hikma Pharmaceuticals USA Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Hikma Pharmaceuticals USA Inc. names for other drugs.
Recalls
- Jan 14, 2020 · Class III · Hikma Pharmaceuticals USA Inc.
Labeling: Incorrect Instructions: Vial label incorrectly instructs healthcare professional to reconstitute product with 16 mL rather than the correct volume of 8 mL of Bacteriostatic Water for Injection with Benzyl Alcohol.
Lots: Lot #: 1901113.1, Exp JUL 2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Methylprednisolone: every company that makes it
- Form
- injection, powder, for solution, intramuscular; intravenous
- Strength
- 500 mg
- Approval
- ANDA ANDA202691
- On the market since
- Jan 1, 2016
- Package NDCs
0143-9850-01- Official label
- DailyMed (National Library of Medicine), updated Feb 13, 2026
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