United States · FDA National Drug Code directory
levofloxacin
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
- 67296-2187_4c5a1f30-3b2b-c5c1-e063-6394a90a0d6a
- Product NDC
- 67296-2187
- Form
- TABLET, FILM COATED
- Composition / generic term
- levofloxacin
- Labeler
- Redpharm Drug
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220110
- Source listing expiry
- 20271231
Source-listed ingredients
- LEVOFLOXACIN — 750 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 TABLET, FILM COATED in 1 BOTTLE (67296-2187-5) · 67296-2187-5
- 7 TABLET, FILM COATED in 1 BOTTLE (67296-2187-7) · 67296-2187-7
- 8 TABLET, FILM COATED in 1 BOTTLE (67296-2187-8) · 67296-2187-8
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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