NDC 65219-016
Ampicillin 500 mg injection, powder, for solution
On the label: Fresenius Kabi USA, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Istituto Biochimico Italiano Giovanni Lorenzini | Aprilia, Italy | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyNov 21, 2024 · 8 inspections, 1 with FDA action |
Product details
- Generic drug
- Ampicillin: every company that makes it
- Form
- injection, powder, for solution, intramuscular; intravenous
- Strength
- 500 mg
- Approval
- ANDA ANDA062719
- On the market since
- Aug 3, 2020
- Package NDCs
65219-016-0165219-016-10- Official label
- DailyMed (National Library of Medicine), updated Oct 21, 2022
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