NDC 0404-9766
Nalbuphine Hydrochloride 20 mg per 1 mL injection
On the label: Henry Schein, Inc.. It's repackaged: Henry Schein, Inc. rebottles it from Somerset Therapeutics, LLC's NDC 70069-662.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Somerset Therapeutics Private Limited | Bengaluru, India | Makes it, tests it, packages it and labels it | Serious problems, FDA actionFeb 21, 2025 · 10 inspections, 4 with FDA action |
Product details
- Generic drug
- Nalbuphine: every company that makes it
- Form
- injection, intramuscular; intravenous; subcutaneous
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA216049
- On the market since
- Dec 10, 2025
- Package NDCs
0404-9766-10- Official label
- DailyMed (National Library of Medicine), updated Apr 27, 2026
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