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
- 85534-0047_56776b15-35d3-3952-e063-6294a90a91e6
- Product NDC
- 85534-0047
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ciprofloxacin Hydrochloride
- Labeler
- HAWAII REPACK, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070426 / 20270228
Source-listed ingredients
- CIPROFLOXACIN HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET, FILM COATED in 1 BOTTLE (85534-0047-0) · 85534-0047-0
- 10 TABLET, FILM COATED in 1 BOTTLE (85534-0047-1) · 85534-0047-1
- 14 TABLET, FILM COATED in 1 BOTTLE (85534-0047-2) · 85534-0047-2
- 20 TABLET, FILM COATED in 1 BOTTLE (85534-0047-3) · 85534-0047-3
- 21 TABLET, FILM COATED in 1 BOTTLE (85534-0047-4) · 85534-0047-4
- 28 TABLET, FILM COATED in 1 BOTTLE (85534-0047-5) · 85534-0047-5
- 30 TABLET, FILM COATED in 1 BOTTLE (85534-0047-6) · 85534-0047-6
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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