United States · FDA National Drug Code directory
Ciprofloxacin Hydrochloride
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
- 67296-0142_510b066c-53c2-1069-e063-6294a90abad5
- Product NDC
- 67296-0142
- Form
- SOLUTION/ DROPS
- Composition / generic term
- Ciprofloxacin Hydrochloride
- Labeler
- Redpharm Drug
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20040507
- 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 (67296-0142-1) / 5 mL in 1 BOTTLE, PLASTIC · 67296-0142-1
- 2 BOTTLE, PLASTIC in 1 CARTON (67296-0142-2) / 5 mL in 1 BOTTLE, PLASTIC · 67296-0142-2
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →