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
- 51655-216_48d2ac12-e669-d797-e063-6394a90aaa7f
- Product NDC
- 51655-216
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ciprofloxacin Hydrochloride
- Labeler
- Northwind Health Company, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230317 / 20270228
Source-listed ingredients
- CIPROFLOXACIN HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-20) · 51655-216-20
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-25) · 51655-216-25
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-52) · 51655-216-52
- 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-53) · 51655-216-53
- 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-84) · 51655-216-84
- 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-87) · 51655-216-87
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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