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
- 71335-2046_0b577d32-713b-4ad8-b6f0-d54f886c38c3
- Product NDC
- 71335-2046
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ciprofloxacin Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070426
- Source listing expiry
- 20261231
Source-listed ingredients
- CIPROFLOXACIN HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 7 TABLET, FILM COATED in 1 BOTTLE (71335-2046-0) · 71335-2046-0
- 14 TABLET, FILM COATED in 1 BOTTLE (71335-2046-1) · 71335-2046-1
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-2046-2) · 71335-2046-2
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-2046-3) · 71335-2046-3
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-2046-4) · 71335-2046-4
- 6 TABLET, FILM COATED in 1 BOTTLE (71335-2046-5) · 71335-2046-5
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-2046-6) · 71335-2046-6
- 28 TABLET, FILM COATED in 1 BOTTLE (71335-2046-7) · 71335-2046-7
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-2046-8) · 71335-2046-8
- 40 TABLET, FILM COATED in 1 BOTTLE (71335-2046-9) · 71335-2046-9
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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