NDC 70121-1609
Methylprednisolone acetate 40 mg per 1 mL injection, suspension
On the label: Amneal Pharmaceuticals LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Amneal Pharmaceuticals Private Limited | Ahmedabad, India | Makes it, tests it, packages it and sterilizes it | No problems foundJun 19, 2024 · 7 inspections |
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 ANDA216502
- On the market since
- Nov 10, 2023
- Package NDCs
70121-1609-170121-1609-5- Official label
- DailyMed (National Library of Medicine), updated Dec 31, 2025
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