NDC 55150-385
Triamcinolone Acetonide 40 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
- Sep 28, 2023 · Class II · Eugia US LLC
Presence of Particulate Matter: A product complaint of a piece of glass was identified in a vial. The piece of glass appears to be roughly 1 cm x 0.5 cm inside the vial.
Lots: Lot #: 3TC22010, Exp 11/30/2024
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Triamcinolone Acetonide: every company that makes it
- Form
- injection, suspension, intra-articular; intramuscular; soft tissue
- Strength
- 40 mg per 1 mL
- Approval
- ANDA ANDA212400
- On the market since
- Jul 5, 2022
- Package NDCs
55150-385-01- Official label
- DailyMed (National Library of Medicine), updated Apr 15, 2025
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