NDC 83939-0002
Ciprofloxacin Hydrochloride 500 mg tablet, film coated
On the label: Verityrx, LLC. It's repackaged: Verityrx, LLC rebottles it from Westminster Pharmaceuticals, LLC's NDC 69367-386.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Westminster Pharmaceuticals, LLC names for other drugs.
Product details
- Generic drug
- Ciprofloxacin: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA076593
- On the market since
- May 23, 2024
- Package NDCs
83939-0002-183939-0002-283939-0002-3- Official label
- DailyMed (National Library of Medicine), updated Nov 3, 2025
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