NDC 70069-027
Buprenorphine Hydrochloride 0.324 mg per 1 mL injection
On the label: Somerset Therapeutics, LLC.
Where it's 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
- Buprenorphine: every company that makes it
- Form
- injection, intramuscular; intravenous
- Strength
- 0.324 mg per 1 mL
- Approval
- ANDA ANDA219302
- On the market since
- Feb 11, 2025
- Package NDCs
70069-027-05- Official label
- DailyMed (National Library of Medicine), updated Feb 11, 2025
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