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
- 63187-990_d0f31dff-c2dd-487d-a329-342765d135e3
- Product NDC
- 63187-990
- Form
- TABLET
- Composition / generic term
- ciprofloxacin
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20040910
- Source listing expiry
- 20261231
Source-listed ingredients
- CIPROFLOXACIN HYDROCHLORIDE — 750 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET in 1 BOTTLE (63187-990-06) · 63187-990-06
- 7 TABLET in 1 BOTTLE (63187-990-07) · 63187-990-07
- 10 TABLET in 1 BOTTLE (63187-990-10) · 63187-990-10
- 14 TABLET in 1 BOTTLE (63187-990-14) · 63187-990-14
- 28 TABLET in 1 BOTTLE (63187-990-28) · 63187-990-28
- 30 TABLET in 1 BOTTLE (63187-990-30) · 63187-990-30
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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