NDC 25021-820
methylprednisolone acetate 40 mg per 1 mL injection, suspension
On the label: Sagent Pharmaceuticals.
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 Sagent Pharmaceuticals names for other drugs.
Recalls
- Apr 25, 2024 · Class II · Sagent Pharmaceuticals
Presence of Particulate Matter: Potential for black particulates in the drug product.
Lots: Lots 5100186, 5100187, 5100188, 5100189, Exp 01/31/2025
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, suspension, intra-articular; intralesional; intramuscular; intrasynovial; soft tissue
- Strength
- 40 mg per 1 mL
- Approval
- ANDA ANDA201835
- On the market since
- Nov 15, 2021
- Package NDCs
25021-820-0525021-820-10- Official label
- DailyMed (National Library of Medicine), updated Mar 2, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?