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NDC 71205-0997-14

Ciprofloxacin Hydrochloride 500 mg/1 TABLET, FILM COATED

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NDC
71205-0997-14
Generic Name
Ciprofloxacin Hydrochloride
Brand Name
Ciprofloxacin
Strength
500 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Package Size
Labeler
Proficient Rx LP

FDA Drug Information

Indications & Usage

1 INDICATIONS AND USAGE Ciprofloxacin Tablets 250 mg, 500 mg, and 750 mg are a fluoroquinolone antibacterial indicated in adults (≥18 years of age) with the following infections caused by designated, susceptible bacteria and in pediatric patients where indicated: • Skin and Skin Structure Infections ( 1.1 ) • Bone and Joint Infections ( 1.2 ) • Complicated Intra-Abdominal Infections ( 1.3 ) • Infectious Diarrhea ( 1.4 ) • Typhoid Fever (Enteric Fever) ( 1.5 ) • Uncomplicated Cervical and Urethra…

Source: FDA. For professional use only. Not a substitute for prescribing information.

Other Ciprofloxacin Hydrochloride NDC Codes

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