Ciprofloxacin Extended Release

Active Ingredient(s): Ciprofloxacin Hydrochloride
FDA Approved: * March 26, 2007
Pharm Company: * REDDYS
Category: Urinary System

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".



Ciprofloxacin Extended Release Overview

Ciprofloxacin (INN) is an antibiotic that can treat a number of bacterial infections. It is a second-generation fluoroquinolone.[2][3] Its spectrum of activity includes most strains of bacterial pathogens responsible for respiratory, urinary tract, gastrointestinal, and abdominal infections, including Gram-negative (Escherichia coli, Haemophilus influenzae, Klebsiella pneumoniae, Legionella pneumophila, Moraxella catarrhalis, Proteus mirabilis, and Pseudomonas aeruginosa), and Gram-positive (...

Read more Ciprofloxacin Extended Release Details
Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Ciprofloxacin

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Possible Dosages for this and Related Drugs:

Ciprofloxacin Hydrochloride
  • ******: 212.6mg + 287.5mg
  • Tablet, Extended Release: 212.6mg + 287.5mg, 425.2mg + 574.9mg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Ciprofloxacin Extended Release: (2 results)

Sorted by National Drug Code
  • 10370-107 Ciprofloxacin Oral Tablet, Film Coated, Extended Release by Par Pharmaceutical, Inc.
  • 10370-108 Ciprofloxacin Oral Tablet, Film Coated, Extended Release by Par Pharmaceutical, Inc.

Other drugs which contain Ciprofloxacin Hydrochloride or a similar ingredient: (1 result)


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