United States · FDA National Drug Code directory

Ciprofloxacin Hydrochloride

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: 69367-387_fe6c75bd-277c-47a8-a218-ab55ac45d453
Product NDC: 69367-387
Form: TABLET, FILM COATED
Composition / generic term: Ciprofloxacin Hydrochloride
Labeler: Westminster Pharmaceuticals, LLC
Marketing category: ANDA
Marketing start / end (source format): 20240523
Source listing expiry: 20271231

Source-listed ingredients

CIPROFLOXACIN HYDROCHLORIDE — 750 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

50 TABLET, FILM COATED in 1 BOTTLE (69367-387-50) · 69367-387-50

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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