NDC 47335-932
vecuronium bromide 1 mg per 1 mL injection, powder, lyophilized, for solution
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Halol, India | Makes it and tests it | Serious problems, FDA actionJun 13, 2025 · 12 inspections, 5 with FDA action |
Recalls
- Jan 3, 2019 · Class I · Sun Pharmaceutical Industries, Inc.
Presence of Particulate Matter: Foreign matter identified as glass detected in Vecuronium Bromide for Injection.
Lots: Lot #: JKS0443A, JKS0444A, JKS0477A, EXP 03/2019 - Jan 3, 2019 · Class I · Sun Pharmaceutical Industries, Inc.
Presence of Particulate Matter: Foreign matter identified as glass detected in Vecuronium Bromide for Injection.
Lots: Lot #: JKS0400A, EXP 03/2019
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Vecuronium: every company that makes it
- Form
- injection, powder, lyophilized, for solution
- Strength
- 1 mg per 1 mL
- Approval
- ANDA ANDA079001
- On the market since
- Dec 15, 2014
- Package NDCs
47335-932-4047335-932-44- Official label
- DailyMed (National Library of Medicine), updated Jul 24, 2026
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