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
- 43063-410_36b0c0b6-8368-77aa-e063-6394a90a0cc7
- Product NDC
- 43063-410
- Form
- TABLET
- Composition / generic term
- ciprofloxacin
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20040910
- Source listing expiry
- 20261231
Source-listed ingredients
- CIPROFLOXACIN HYDROCHLORIDE — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET in 1 BOTTLE, PLASTIC (43063-410-06) · 43063-410-06
- 10 TABLET in 1 BOTTLE, PLASTIC (43063-410-10) · 43063-410-10
- 12 TABLET in 1 BOTTLE, PLASTIC (43063-410-12) · 43063-410-12
- 14 TABLET in 1 BOTTLE, PLASTIC (43063-410-14) · 43063-410-14
- 20 TABLET in 1 BOTTLE, PLASTIC (43063-410-20) · 43063-410-20
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 →