NDC 59651-589

Nadolol 20 mg tablet

On the label: Aurobindo Pharma Limited.

India: 1

Where it's made

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

Product details

Generic drug
Nadolol: every company that makes it
Form
tablet, oral
Strength
20 mg
Approval
ANDA ANDA201893
On the market since
Jun 7, 2022
Package NDCs
59651-589-01
Official label
DailyMed (National Library of Medicine), updated Jan 10, 2024

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