# Ciprofloxacin

NDC: 43063-923
Generic name: Ciprofloxacin Hydrochloride
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20091010

FDA application: ANDA076126

## Active ingredients

- CIPROFLOXACIN HYDROCHLORIDE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43063-923"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-923
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cfda82e4-8660-447e-a881-b87165a31e9a