NDC 54868-5757
Cefprozil 250 mg per 5 mL powder, for suspension
On the label: Physicians Total Care, Inc.. It's repackaged: Physicians Total Care, Inc. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-402.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Mandideep, India | Makes it | Serious problems, FDA actionNov 23, 2022 · 6 inspections, 3 with FDA action |
Recalls
- Mar 26, 2021 · Class II · Lupin Pharmaceuticals Inc.
Superpotent Drug
Lots: Lot Numbers: a) F801122, exp. date June 2021; b) F801123, exp. date June 2021; c) F801124, exp. date June 2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Cefprozil: every company that makes it
- Form
- powder, for suspension
- Strength
- 250 mg per 5 mL
- Approval
- ANDA ANDA065261
- On the market since
- Feb 5, 2007
- Package NDCs
54868-5757-068180-402-03- Official label
- DailyMed (National Library of Medicine), updated Dec 8, 2010
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