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
- 72789-108_4d622f0c-9f42-a920-e063-6394a90a0f73
- Product NDC
- 72789-108
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ciprofloxacin
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20040609
- Source listing expiry
- 20271231
Source-listed ingredients
- CIPROFLOXACIN HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-02) · 72789-108-02
- 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-10) · 72789-108-10
- 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-14) · 72789-108-14
- 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-20) · 72789-108-20
- 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-28) · 72789-108-28
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-30) · 72789-108-30
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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