NDC 54348-662
ciprofloxacin 250 mg tablet
On the label: PharmPak, Inc.. It's repackaged: PharmPak, Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 16571-411.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Unique Pharmaceutical Laboratories | Bharuch, India | Makes it and tests it | Problems found, fixed voluntarilyOct 23, 2022 · 6 inspections |
| Unique Pharmaceutical Laboratories | Bharuch, India | Makes it and tests it | No problems foundMar 7, 2025 · 2 inspections |
Recalls
- Mar 9, 2012 · Class III · Pack Pharmaceuticals
Labeling Illegible: Missing Label; The voluntary recall of the aforementioned batch of product is being initiated due to two bottles missing container labels.
Lots: Lot #: : PUB1040, Exp 08/2015
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ciprofloxacin: every company that makes it
- Form
- tablet, oral
- Strength
- 250 mg
- Approval
- ANDA ANDA076639
- On the market since
- Jul 10, 2019
- Package NDCs
54348-662-0654348-662-14- Official label
- DailyMed (National Library of Medicine), updated Oct 9, 2022
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