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
- 72789-519_3f92e4b4-bd66-8f5d-e063-6394a90aa46d
- Product NDC
- 72789-519
- Form
- TABLET
- Composition / generic term
- Ciprofolxacin
- Labeler
- PD-Rx Pharmaceuticals, 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
- 6 TABLET in 1 BOTTLE, PLASTIC (72789-519-06) · 72789-519-06
- 10 TABLET in 1 BOTTLE, PLASTIC (72789-519-10) · 72789-519-10
- 12 TABLET in 1 BOTTLE, PLASTIC (72789-519-12) · 72789-519-12
- 14 TABLET in 1 BOTTLE, PLASTIC (72789-519-14) · 72789-519-14
- 20 TABLET in 1 BOTTLE, PLASTIC (72789-519-20) · 72789-519-20
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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