NDC 65862-603

Moxifloxacin Hydrochloride 400 mg tablet, film coated

On the label: Aurobindo Pharma Limited.

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
65862-603-10 65862-603-30 65862-603-55 65862-603-99
Official label
DailyMed (National Library of Medicine), updated Sep 1, 2025

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