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
- 70069-081_1a4f432a-c2b2-46bc-88fc-7379c2bbd0a2
- Product NDC
- 70069-081
- Form
- SOLUTION/ DROPS
- Composition / generic term
- Moxifloxacin Hydrochloride
- Labeler
- Somerset Therapeutics, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241125
- Source listing expiry
- 20261231
Source-listed ingredients
- MOXIFLOXACIN HYDROCHLORIDE — 5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (70069-081-01) / 3 mL in 1 BOTTLE · 70069-081-01
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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