NDC 70069-048
Sodium acetate anhydrous 164 mg per 1 mL solution, concentrate
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
- Acetate Ion: every company that makes it
- Form
- solution, concentrate, intravenous
- Strength
- 164 mg per 1 mL
- Approval
- ANDA ANDA219826
- On the market since
- Oct 23, 2025
- Package NDCs
70069-048-20- Official label
- DailyMed (National Library of Medicine), updated Oct 21, 2025
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