NDC 43386-038
Voriconazole 40 mg per 1 mL powder, for suspension
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Novel Laboratories, Inc. | Somerset, NJ, United States | Makes it and tests it | Problems found, fixed voluntarilyApr 17, 2026 · 15 inspections, 1 with FDA action |
Recalls
- Feb 5, 2024 · Class II · Lupin Pharmaceuticals Inc.
Labeling: Incorrect or Missing Package Insert
Lots: Lot#: S200756; Exp. 10/2024 Lot#: S300218; Exp. 04/2025 Lot#: S300633; Exp. 09/2025
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Voriconazole: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 40 mg per 1 mL
- Approval
- ANDA ANDA206799
- On the market since
- Jun 1, 2016
- Package NDCs
43386-038-60- Official label
- DailyMed (National Library of Medicine), updated Sep 26, 2025
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