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
- 50090-7843_56da4ad6-dcd2-4df7-b174-e78c8e0127b6
- Product NDC
- 50090-7843
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ciprofloxacin Hydrochloride
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240523
- Source listing expiry
- 20271231
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 (50090-7843-0) · 50090-7843-0
- 14 TABLET, FILM COATED in 1 BOTTLE (50090-7843-1) · 50090-7843-1
- 6 TABLET, FILM COATED in 1 BOTTLE (50090-7843-3) · 50090-7843-3
- 28 TABLET, FILM COATED in 1 BOTTLE (50090-7843-4) · 50090-7843-4
- 10 TABLET, FILM COATED in 1 BOTTLE (50090-7843-5) · 50090-7843-5
- 30 TABLET, FILM COATED in 1 BOTTLE (50090-7843-7) · 50090-7843-7
- 1 TABLET, FILM COATED in 1 BOTTLE (50090-7843-8) · 50090-7843-8
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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