NDC 72789-330

Ciprofloxacin 500 mg tablet, film coated

On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-077.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMedchal, IndiaMakes it and tests it Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Ciprofloxacin: every company that makes it
Form
tablet, film coated, oral
Strength
500 mg
Approval
ANDA ANDA077859
On the market since
Apr 26, 2007
Package NDCs
72789-330-28
Official label
DailyMed (National Library of Medicine), updated Jun 9, 2026

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