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
- 68084-722_55a1e3ca-d771-b7e8-e063-6294a90ac3ec
- Product NDC
- 68084-722
- Form
- TABLET, FILM COATED
- Composition / generic term
- Moxifloxacin Hydrochloride
- Labeler
- American Health Packaging
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140319
- Source listing expiry
- 20271231
Source-listed ingredients
- MOXIFLOXACIN HYDROCHLORIDE — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 50 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-722-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-722-11) · 68084-722-65
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 →