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
- 55111-279_c51f53eb-2f01-93dc-e7e6-695b20b639ce
- Product NDC
- 55111-279
- Form
- TABLET, FILM COATED
- Composition / generic term
- Levofloxacin
- Labeler
- Dr. Reddy's Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110620
- Source listing expiry
- 20261231
Source-listed ingredients
- LEVOFLOXACIN — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (55111-279-01) · 55111-279-01
- 500 TABLET, FILM COATED in 1 BOTTLE (55111-279-05) · 55111-279-05
- 30 TABLET, FILM COATED in 1 BOTTLE (55111-279-30) · 55111-279-30
- 50 TABLET, FILM COATED in 1 BOTTLE (55111-279-50) · 55111-279-50
- 10 BLISTER PACK in 1 CARTON (55111-279-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-279-79) · 55111-279-78
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →