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
- 71335-3173_15b15a3c-847e-4df1-8f5e-131ff4290a6d
- Product NDC
- 71335-3173
- Form
- TABLET, FILM COATED
- Composition / generic term
- levofloxacin
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220110
- Source listing expiry
- 20271231
Source-listed ingredients
- LEVOFLOXACIN — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-3173-1) · 71335-3173-1
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-3173-2) · 71335-3173-2
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-3173-3) · 71335-3173-3
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-3173-4) · 71335-3173-4
- 14 TABLET, FILM COATED in 1 BOTTLE (71335-3173-5) · 71335-3173-5
- 3 TABLET, FILM COATED in 1 BOTTLE (71335-3173-6) · 71335-3173-6
- 5 TABLET, FILM COATED in 1 BOTTLE (71335-3173-7) · 71335-3173-7
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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