United States · FDA National Drug Code directory
Ciprofloxacin and Dexamethasone
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
- 0781-6186_39a8b845-aa32-4c9d-bef8-18cea1ef7bc9
- Product NDC
- 0781-6186
- Form
- SUSPENSION/ DROPS
- Composition / generic term
- ciprofloxacin and dexamethasone
- Labeler
- Sandoz Inc
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20200810
- Source listing expiry
- 20261231
Source-listed ingredients
- CIPROFLOXACIN HYDROCHLORIDE — 3 mg/mL
- DEXAMETHASONE — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, DROPPER in 1 CARTON (0781-6186-67) / 7.5 mL in 1 BOTTLE, DROPPER · 0781-6186-67
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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