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
- 76420-928_5534e308-fd71-8890-e063-6294a90ab044
- Product NDC
- 76420-928
- Form
- TABLET
- Composition / generic term
- Ciprofolxacin
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231001
- Source listing expiry
- 20271231
Source-listed ingredients
- CIPROFLOXACIN HYDROCHLORIDE — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (76420-928-01) · 76420-928-01
- 14 TABLET in 1 BOTTLE (76420-928-14) · 76420-928-14
- 20 TABLET in 1 BOTTLE (76420-928-20) · 76420-928-20
- 30 TABLET in 1 BOTTLE (76420-928-30) · 76420-928-30
- 60 TABLET in 1 BOTTLE (76420-928-60) · 76420-928-60
- 90 TABLET in 1 BOTTLE (76420-928-90) · 76420-928-90
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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