NDC 0404-9992
Methocarbamol 1000 mg per 10 mL injection, solution
On the label: Henry Schein, Inc.. It's repackaged: Henry Schein, Inc. rebottles it from AuroMedics Pharma LLC's NDC 55150-223.
Where the pills inside were 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 15, 2024 · Class I · Eugia US LLC
Presence of Particulate Matter
Lots: Lot #: 3MC23011, Exp 11/30/2026
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Methocarbamol: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 1000 mg per 10 mL
- Approval
- ANDA ANDA206128
- On the market since
- Apr 6, 2023
- Package NDCs
0404-9992-10- Official label
- DailyMed (National Library of Medicine), updated Oct 5, 2026
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