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
- 71335-2265_477d7d9e-1637-4c49-b588-f1da546a67f0
- Product NDC
- 71335-2265
- Form
- TABLET, FILM COATED
- Composition / generic term
- levofloxacin
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220110
- Source listing expiry
- 20261231
Source-listed ingredients
- LEVOFLOXACIN — 750 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 TABLET, FILM COATED in 1 BOTTLE (71335-2265-0) · 71335-2265-0
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-2265-1) · 71335-2265-1
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-2265-2) · 71335-2265-2
- 7 TABLET, FILM COATED in 1 BOTTLE (71335-2265-3) · 71335-2265-3
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-2265-4) · 71335-2265-4
- 5 TABLET, FILM COATED in 1 BOTTLE (71335-2265-5) · 71335-2265-5
- 14 TABLET, FILM COATED in 1 BOTTLE (71335-2265-6) · 71335-2265-6
- 28 TABLET, FILM COATED in 1 BOTTLE (71335-2265-7) · 71335-2265-7
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-2265-8) · 71335-2265-8
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-2265-9) · 71335-2265-9
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 →