NDC 63187-017
ciprofloxacin 500 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP 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
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels 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
- 500 mg
- Approval
- ANDA ANDA076639
- On the market since
- Sep 10, 2004
- Package NDCs
63187-017-0663187-017-1063187-017-1463187-017-2063187-017-2863187-017-3063187-017-6063187-017-90- Official label
- DailyMed (National Library of Medicine), updated Jun 1, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?