NDC 55150-314
Methylprednisolone Acetate 80 mg per 1 mL injection, suspension
On the label: AuroMedics Pharma LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
Recalls
- Feb 20, 2024 · Class II · Eugia US LLC
Failed Dissolution Specifications
Lots: Lot #: 3MA23001, 3MA23002, 3MA23003, Exp 3/31/2025
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; soft tissue
- Strength
- 80 mg per 1 mL
- Approval
- ANDA ANDA211930
- On the market since
- Apr 13, 2023
- Package NDCs
55150-314-0155150-314-25- Official label
- DailyMed (National Library of Medicine), updated Apr 21, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?