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: 51407-165_2ee94e9b-43b8-e3d5-e063-6394a90ae89b
Product NDC: 51407-165
Form: TABLET, FILM COATED
Composition / generic term: Ciprofloxacin Hydrochloride
Labeler: Golden State Medical Supply, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20040609
Source listing expiry: 20261231

Source-listed ingredients

CIPROFLOXACIN HYDROCHLORIDE — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET, FILM COATED in 1 BOTTLE (51407-165-01) · 51407-165-01
20 TABLET, FILM COATED in 1 BOTTLE (51407-165-20) · 51407-165-20
28 TABLET, FILM COATED in 1 BOTTLE (51407-165-28) · 51407-165-28

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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