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
- 68071-3699_4656418d-1f8e-b3bf-e063-6294a90a2401
- Product NDC
- 68071-3699
- Form
- TABLET
- Composition / generic term
- Ciprofolxacin
- Labeler
- NuCare Pharmaceutical, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231001
- Source listing expiry
- 20261231
Source-listed ingredients
- CIPROFLOXACIN HYDROCHLORIDE — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE (68071-3699-1) · 68071-3699-1
- 20 TABLET in 1 BOTTLE (68071-3699-2) · 68071-3699-2
- 30 TABLET in 1 BOTTLE (68071-3699-3) · 68071-3699-3
- 6 TABLET in 1 BOTTLE (68071-3699-6) · 68071-3699-6
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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