United States · FDA National Drug Code directory
Moxifloxacin Hydrochloride
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
- 71335-2815_6ac508d3-c5c6-49b1-ab21-56896601f8ad
- Product NDC
- 71335-2815
- Form
- TABLET, FILM COATED
- Composition / generic term
- Moxifloxacin Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140304
- Source listing expiry
- 20261231
Source-listed ingredients
- MOXIFLOXACIN HYDROCHLORIDE — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 7 TABLET, FILM COATED in 1 BOTTLE (71335-2815-1) · 71335-2815-1
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-2815-2) · 71335-2815-2
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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