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
- 71205-997_1c1b4148-3301-4ab7-8955-667658b4c133
- Product NDC
- 71205-997
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ciprofloxacin Hydrochloride
- Labeler
- Proficient Rx LP
- 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 (71205-997-00) · 71205-997-00
- 10 TABLET, FILM COATED in 1 BOTTLE (71205-997-10) · 71205-997-10
- 14 TABLET, FILM COATED in 1 BOTTLE (71205-997-14) · 71205-997-14
- 20 TABLET, FILM COATED in 1 BOTTLE (71205-997-20) · 71205-997-20
- 30 TABLET, FILM COATED in 1 BOTTLE (71205-997-30) · 71205-997-30
- 500 TABLET, FILM COATED in 1 BOTTLE (71205-997-55) · 71205-997-55
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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