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
- 72162-1741_d2a899a6-43fe-42f7-b1b5-4731f74e3792
- Product NDC
- 72162-1741
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ciprofloxacin Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20091010
- 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 (72162-1741-1) · 72162-1741-1
- 14 TABLET, FILM COATED in 1 BOTTLE (72162-1741-2) · 72162-1741-2
- 30 TABLET, FILM COATED in 1 BOTTLE (72162-1741-3) · 72162-1741-3
- 20 TABLET, FILM COATED in 1 BOTTLE (72162-1741-4) · 72162-1741-4
- 500 TABLET, FILM COATED in 1 BOTTLE (72162-1741-5) · 72162-1741-5
- 60 TABLET, FILM COATED in 1 BOTTLE (72162-1741-6) · 72162-1741-6
- 10 TABLET, FILM COATED in 1 BOTTLE (72162-1741-7) · 72162-1741-7
- 120 TABLET, FILM COATED in 1 BOTTLE (72162-1741-8) · 72162-1741-8
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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