Drugplain

NDC 70934-965-14

Ciprofloxacin 500 mg/1

Ciprofloxacin Hydrochloride · TABLET, FILM COATED

No Recall History

Ciprofloxacin is a tablet, film coated containing ciprofloxacin hydrochloride at a strength of 500 mg/1. Manufactured by Denton Pharma, Inc. DBA Northwind Pharmaceuticals.

Key Facts

Brand Name
Ciprofloxacin
Generic Name
Ciprofloxacin Hydrochloride
NDC Code (Package)
70934-965-14
NDC Code (Product)
70934-965
Manufacturer
Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Strength
500 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA076126
Marketing Start
05/02/2022

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.