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
- 71205-749_6b5fe0aa-c74f-42f3-a84a-1cb16009aa80
- Product NDC
- 71205-749
- Form
- TABLET, COATED
- Composition / generic term
- Ciprofloxacin
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200812
- Source listing expiry
- 20261231
Source-listed ingredients
- CIPROFLOXACIN HYDROCHLORIDE — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 TABLET, COATED in 1 BOTTLE (71205-749-05) · 71205-749-05
- 6 TABLET, COATED in 1 BOTTLE (71205-749-06) · 71205-749-06
- 10 TABLET, COATED in 1 BOTTLE (71205-749-10) · 71205-749-10
- 14 TABLET, COATED in 1 BOTTLE (71205-749-14) · 71205-749-14
- 20 TABLET, COATED in 1 BOTTLE (71205-749-20) · 71205-749-20
- 28 TABLET, COATED in 1 BOTTLE (71205-749-28) · 71205-749-28
- 30 TABLET, COATED in 1 BOTTLE (71205-749-30) · 71205-749-30
- 60 TABLET, COATED in 1 BOTTLE (71205-749-60) · 71205-749-60
- 90 TABLET, COATED in 1 BOTTLE (71205-749-90) · 71205-749-90
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →