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
- 82868-070_476ba1ad-f80f-8ff0-e063-6294a90a11f2
- Product NDC
- 82868-070
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ciprofloxacin Hydrochloride
- Labeler
- Northwind Health Company, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250121 / 20270131
Source-listed ingredients
- CIPROFLOXACIN HYDROCHLORIDE — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-070-14) · 82868-070-14
- 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-070-20) · 82868-070-20
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 →