NDC 57237-156

Moxifloxacin Hydrochloride 400 mg tablet, film coated

On the label: Rising Pharma Holdings, Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMahabubnagar, IndiaMakes it and tests it Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action

Product details

Generic drug
Moxifloxacin: every company that makes it
Form
tablet, film coated, oral
Strength
400 mg
Approval
ANDA ANDA202632
On the market since
Mar 4, 2014
Package NDCs
57237-156-30
Official label
DailyMed (National Library of Medicine), updated Oct 10, 2025

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