United States · FDA National Drug Code directory
CIPROFLOXACIN
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 72189-111_4c499af5-b74b-2799-e063-6294a90a7054
- Product NDC
- 72189-111
- Form
- TABLET, FILM COATED
- Composition / generic term
- ciprofloxacin hydrochloride
- Labeler
- DIRECT RX
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200612 / 20270228
Source-listed ingredients
- CIPROFLOXACIN HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET, FILM COATED in 1 BOTTLE (72189-111-10) · 72189-111-10
- 14 TABLET, FILM COATED in 1 BOTTLE (72189-111-14) · 72189-111-14
- 20 TABLET, FILM COATED in 1 BOTTLE (72189-111-20) · 72189-111-20
- 30 TABLET, FILM COATED in 1 BOTTLE (72189-111-30) · 72189-111-30
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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