United States · FDA National Drug Code directory
Moxifloxacin
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
- 63323-850_4070f637-059f-4e3d-8cf3-e5256a46ff3e
- Product NDC
- 63323-850
- Form
- INJECTION, SOLUTION
- Composition / generic term
- MOXIFLOXACIN HYDROCHLORIDE
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20150318
- Source listing expiry
- 20261231
Source-listed ingredients
- MOXIFLOXACIN HYDROCHLORIDE — 400 mg/250mL
These values do not establish equivalence or a dose recommendation.
Packages
- 12 BAG in 1 CASE (63323-850-04) / 250 mL in 1 BAG (63323-850-74) · 63323-850-04
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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