NDC 43063-767
ciprofloxacin 750 mg tablet
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 16571-413.
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 |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
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
- 750 mg
- Approval
- ANDA ANDA076639
- On the market since
- Sep 10, 2004
- Package NDCs
43063-767-28- Official label
- DailyMed (National Library of Medicine), updated Jun 4, 2025
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