NDC 70934-045
ciprofloxacin 500 mg tablet
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Rising Pharma Holdings, Inc.'s NDC 16571-412.
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 |
Repackaging site
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · 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
- Strength
- 500 mg
- Approval
- ANDA ANDA076639
- On the market since
- Nov 21, 2017
- Package NDCs
70934-045-0670934-045-1070934-045-1470934-045-2070934-045-3070934-045-60- Official label
- DailyMed (National Library of Medicine), updated Jan 21, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?