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
- 71205-002_a630f88d-800c-400f-9da4-1b26c0ee1f85
- Product NDC
- 71205-002
- Form
- TABLET, FILM COATED
- Composition / generic term
- Levofloxacin
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150109
- Source listing expiry
- 20261231
Source-listed ingredients
- LEVOFLOXACIN — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 TABLET, FILM COATED in 1 BOTTLE (71205-002-03) · 71205-002-03
- 5 TABLET, FILM COATED in 1 BOTTLE (71205-002-05) · 71205-002-05
- 7 TABLET, FILM COATED in 1 BOTTLE (71205-002-07) · 71205-002-07
- 10 TABLET, FILM COATED in 1 BOTTLE (71205-002-10) · 71205-002-10
- 12 TABLET, FILM COATED in 1 BOTTLE (71205-002-12) · 71205-002-12
- 14 TABLET, FILM COATED in 1 BOTTLE (71205-002-14) · 71205-002-14
- 21 TABLET, FILM COATED in 1 BOTTLE (71205-002-21) · 71205-002-21
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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