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: 72789-350_4bbf366b-77ca-fc66-e063-6394a90aebf4
Product NDC: 72789-350
Form: TABLET, FILM COATED
Composition / generic term: Moxifloxacin Hydrochloride
Labeler: PD-Rx Pharmaceuticals, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20140304
Source listing expiry: 20271231

Source-listed ingredients

MOXIFLOXACIN HYDROCHLORIDE — 400 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-350-10) · 72789-350-10

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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