NDC 68180-401
Cefprozil 125 mg per 5 mL powder, for suspension
On the label: Lupin Pharmaceuticals, Inc..
Where it's 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, oral
- Strength
- 125 mg per 5 mL
- Approval
- ANDA ANDA065261
- On the market since
- Dec 1, 2005
- Package NDCs
68180-401-0168180-401-0268180-401-03- Official label
- DailyMed (National Library of Medicine), updated Oct 10, 2025
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