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
- 85534-0075_566c6b87-1aa7-7ddc-e063-6394a90acd3b
- Product NDC
- 85534-0075
- Form
- SOLUTION
- Composition / generic term
- Ciprofloxacin
- Labeler
- HAWAII REPACK, INC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181101
- Source listing expiry
- 20271231
Source-listed ingredients
- CIPROFLOXACIN HYDROCHLORIDE — 3 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (85534-0075-0) / 2.5 mL in 1 BOTTLE, PLASTIC · 85534-0075-0
- 1 BOTTLE, PLASTIC in 1 CARTON (85534-0075-1) / 5 mL in 1 BOTTLE, PLASTIC · 85534-0075-1
- 1 BOTTLE, PLASTIC in 1 CARTON (85534-0075-2) / 10 mL in 1 BOTTLE, PLASTIC · 85534-0075-2
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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