NDC 70069-752
Bupivacaine hydrochloride 2.5 mg per 1 mL injection, solution
On the label: Somerset Therapeutics, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Maiva Pharma Private Limited | Hosur, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 29, 2022 · 1 inspection |
Product details
- Generic drug
- Bupivacaine: every company that makes it
- Form
- injection, solution, infiltration; perineural
- Strength
- 2.5 mg per 1 mL
- Approval
- ANDA ANDA217792
- On the market since
- Nov 27, 2023
- Package NDCs
70069-752-0170069-752-1070069-752-25- Official label
- DailyMed (National Library of Medicine), updated Jun 20, 2024
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