NDC 0143-9754
Methylprednisolone Sodium Succinate 125 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.
Product details
- Generic drug
- Methylprednisolone: every company that makes it
- Form
- injection, powder, for solution, intramuscular; intravenous
- Strength
- 125 mg
- Approval
- ANDA ANDA203125
- On the market since
- Sep 26, 2022
- Package NDCs
0143-9754-010143-9754-25- Official label
- DailyMed (National Library of Medicine), updated Feb 13, 2026
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