NDC 69367-387-50
Ciprofloxacin Hydrochloride 750 mg/1
Ciprofloxacin Hydrochloride · TABLET, FILM COATED
Ciprofloxacin hydrochloride is an antibiotic used to treat bacterial infections, including urinary tract infections, respiratory infections, and skin infections. This oral tablet comes in a 750 mg strength and requires a prescription.
Key Facts
- Brand Name
- Ciprofloxacin Hydrochloride
- Generic Name
- Ciprofloxacin Hydrochloride
- NDC Code (Package)
69367-387-50- NDC Code (Product)
69367-387- Manufacturer
- Westminster Pharmaceuticals, LLC
- Strength
- 750 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA076593
- Marketing Start
- 05/23/2024
Recall History
No Recall HistoryView Full Drug Page
Ciprofloxacin Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.