NDC 51662-1560
Ampicillin 2 g 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 AuroMedics Pharma LLC's NDC 55150-114.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Serious problems, FDA actionSep 5, 2025 · 8 inspections, 1 with FDA action |
| Eugia Sez Private Limited | Mahabubnagar, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMar 1, 2019 · 2 inspections |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Recalls
- Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
cGMP deviations: Temperature abuse
Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ampicillin: every company that makes it
- Form
- injection, powder, for solution, intravenous
- Strength
- 2 g
- Approval
- ANDA ANDA065499
- On the market since
- Jul 31, 2022
- Package NDCs
51662-1560-251662-1560-3- Official label
- DailyMed (National Library of Medicine), updated Jan 14, 2024
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