NDC 51662-1595
Ampicillin 250 mg injection, powder, for solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Fresenius Kabi USA, LLC's NDC 65219-014.
Where the pills inside were 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 |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Ampicillin: every company that makes it
- Form
- injection, powder, for solution, intramuscular; intravenous
- Strength
- 250 mg
- Approval
- ANDA ANDA062719
- On the market since
- Aug 18, 2022
- Package NDCs
51662-1595-251662-1595-3- Official label
- DailyMed (National Library of Medicine), updated Jan 28, 2024
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